geneid | 22993 |
---|---|
ensemblid | ENSG00000113716.13 |
hgncid | 28982 |
symbol | HMGXB3 |
name | HMG-box containing 3 |
refseq_nuc | NM_014983.3 |
refseq_prot | NP_055798.3 |
ensembl_nuc | ENST00000502717.6 |
ensembl_prot | ENSP00000421917.1 |
mane_status | MANE Select |
chr | chr5 |
start | 150000739 |
end | 150053128 |
strand | + |
ver | v1.2 |
region | chr5:150000739-150053128 |
region5000 | chr5:149995739-150058128 |
regionname0 | HMGXB3_chr5_150000739_150053128 |
regionname5000 | HMGXB3_chr5_149995739_150058128 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1292 | 180 | 72 | 29 | 55 | 4 | 19 | 40 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0002 | 1/0 | 1292 | 99 | 0 | 17 | 60 | 3 | 18 | 52 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0003 | 0/0 | 1292 | 42 | 4 | 15 | 21 | 2 | 0 | 15 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0004 | 0/0 | 1292 | 33 | 8 | 5 | 16 | 0 | 4 | 14 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0005 | 0/0 | 1292 | 8 | 5 | 3 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0006 | 0/0 | 1292 | 4 | 1 | 1 | 1 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0007 | 0/0 | 1292 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0008 | 0/0 | 1292 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0009 | 0/0 | 1292 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0010 | 0/0 | 1292 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0011 | 0/0 | 1292 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0012 | 0/0 | 1292 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0013 | 0/0 | 1292 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0014 | 0/0 | 1292 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0015 | 0/0 | 1292 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0016 | 0/0 | 1292 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0017 | 0/0 | 1292 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 3879 | 123 | 21 | 26 | 55 | 3 | 17 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
c0002 | 1/0 | 3879 | 96 | 0 | 16 | 58 | 3 | 18 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
c0003 | 0/0 | 3879 | 52 | 48 | 3 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
c0004 | 0/0 | 3879 | 39 | 4 | 15 | 18 | 2 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
c0005 | 0/0 | 3879 | 28 | 8 | 1 | 16 | 0 | 3 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
c0006 | 0/0 | 3879 | 8 | 5 | 3 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
c0007 | 0/0 | 3879 | 5 | 0 | 4 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
c0008 | 0/0 | 3879 | 4 | 1 | 1 | 1 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
c0009 | 0/0 | 3879 | 3 | 3 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
c0010 | 0/0 | 3879 | 3 | 0 | 0 | 3 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
c0011 | 0/0 | 3879 | 2 | 2 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
c0012 | 0/0 | 3879 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
c0013 | 0/0 | 3879 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
c0014 | 0/0 | 3879 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
c0015 | 0/0 | 3879 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
c0016 | 0/0 | 3879 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
c0017 | 0/0 | 3879 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
c0018 | 0/0 | 3879 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
c0019 | 0/0 | 3879 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
c0020 | 0/0 | 3879 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
c0021 | 0/0 | 3879 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
c0022 | 0/0 | 3879 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
c0023 | 0/0 | 3879 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
c0024 | 0/0 | 3879 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
c0025 | 0/0 | 3879 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
c0026 | 0/0 | 3879 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
c0027 | 0/0 | 3879 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
c0028 | 0/0 | 3879 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1380 | 104 | 27 | 9 | 58 | 0 | 10 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0002 | 1/0 | 1380 | 88 | 0 | 21 | 47 | 3 | 16 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0003 | 0/1 | 1380 | 52 | 7 | 12 | 16 | 4 | 12 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0004 | 0/0 | 1380 | 41 | 8 | 11 | 22 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0005 | 0/0 | 1380 | 37 | 29 | 3 | 3 | 0 | 2 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0006 | 0/0 | 1380 | 9 | 8 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0007 | 0/0 | 1380 | 6 | 0 | 4 | 0 | 2 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0008 | 0/0 | 1380 | 6 | 6 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0009 | 0/0 | 1380 | 5 | 2 | 3 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0010 | 0/0 | 1380 | 5 | 0 | 0 | 5 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0011 | 0/0 | 1380 | 4 | 4 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0012 | 0/0 | 1380 | 2 | 0 | 1 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0013 | 0/0 | 1380 | 2 | 1 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0014 | 0/0 | 1380 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0015 | 0/0 | 1380 | 2 | 1 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0016 | 0/0 | 1380 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0017 | 0/0 | 1380 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0018 | 0/0 | 1380 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0019 | 0/0 | 1380 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0020 | 0/0 | 1380 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0021 | 0/0 | 1380 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0022 | 0/0 | 1380 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0023 | 0/0 | 1380 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0024 | 0/0 | 1380 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0025 | 0/0 | 1380 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0026 | 0/0 | 1380 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0027 | 0/0 | 1380 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0028 | 0/0 | 1380 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0029 | 0/0 | 1380 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
t0030 | 0/0 | 1380 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0002 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0003 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0007 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0011 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0027 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0028 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0029 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0066 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3879 | 123 | 21 | 26 | 55 | 3 | 17 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0003 | 0/0 | 3879 | 52 | 48 | 3 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0017 | 0/0 | 3879 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0018 | 0/0 | 3879 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0019 | 0/0 | 3879 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0021 | 0/0 | 3879 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0026 | 0/0 | 3879 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0002c0002 | 1/0 | 3879 | 96 | 0 | 16 | 58 | 3 | 18 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0002c0013 | 0/0 | 3879 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0002c0014 | 0/0 | 3879 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0002c0023 | 0/0 | 3879 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0003c0004 | 0/0 | 3879 | 39 | 4 | 15 | 18 | 2 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0003c0010 | 0/0 | 3879 | 3 | 0 | 0 | 3 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0004c0005 | 0/0 | 3879 | 28 | 8 | 1 | 16 | 0 | 3 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0004c0007 | 0/0 | 3879 | 5 | 0 | 4 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0005c0006 | 0/0 | 3879 | 8 | 5 | 3 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0006c0008 | 0/0 | 3879 | 4 | 1 | 1 | 1 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0007c0009 | 0/0 | 3879 | 3 | 3 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0008c0011 | 0/0 | 3879 | 2 | 2 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0009c0028 | 0/0 | 3879 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0010c0027 | 0/0 | 3879 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0011c0012 | 0/0 | 3879 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0012c0020 | 0/0 | 3879 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0013c0024 | 0/0 | 3879 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0014c0016 | 0/0 | 3879 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0015c0015 | 0/0 | 3879 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0016c0022 | 0/0 | 3879 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0017c0025 | 0/0 | 3879 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5258 | 61 | 10 | 9 | 35 | 0 | 7 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0001t0002 | 0/0 | 5258 | 5 | 0 | 1 | 2 | 0 | 2 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0001t0003 | 0/1 | 5258 | 43 | 4 | 12 | 15 | 3 | 8 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0001t0005 | 0/0 | 5258 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0001t0006 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0001t0011 | 0/0 | 5258 | 4 | 4 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0001t0012 | 0/0 | 5258 | 2 | 0 | 1 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0001t0013 | 0/0 | 5258 | 2 | 1 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0001t0021 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0001t0026 | 0/0 | 5258 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0001t0027 | 0/0 | 5258 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0001t0029 | 0/0 | 5258 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0003t0001 | 0/0 | 5258 | 9 | 9 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0003t0003 | 0/0 | 5258 | 2 | 2 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0003t0005 | 0/0 | 5258 | 25 | 22 | 3 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0003t0006 | 0/0 | 5258 | 7 | 6 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0003t0008 | 0/0 | 5258 | 6 | 6 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0003t0019 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0003t0020 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0003t0030 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0017t0003 | 0/0 | 5258 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0018t0005 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0019t0005 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0021t0006 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0001c0026t0003 | 0/0 | 5258 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0002c0002t0001 | 0/0 | 5258 | 6 | 0 | 0 | 6 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0002c0002t0002 | 1/0 | 5258 | 74 | 0 | 15 | 43 | 2 | 13 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0002c0002t0003 | 0/0 | 5258 | 3 | 0 | 0 | 1 | 0 | 2 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0002c0002t0005 | 0/0 | 5258 | 3 | 0 | 0 | 2 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0002c0002t0010 | 0/0 | 5258 | 5 | 0 | 0 | 5 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0002c0002t0015 | 0/0 | 5258 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0002c0002t0016 | 0/0 | 5258 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0002c0002t0022 | 0/0 | 5258 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0002c0002t0023 | 0/0 | 5258 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0002c0002t0025 | 0/0 | 5258 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0002c0013t0002 | 0/0 | 5258 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0002c0014t0002 | 0/0 | 5258 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0002c0023t0014 | 0/0 | 5258 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0003c0004t0004 | 0/0 | 5258 | 32 | 4 | 10 | 18 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0003c0004t0007 | 0/0 | 5258 | 6 | 0 | 4 | 0 | 2 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0003c0004t0017 | 0/0 | 5258 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0003c0010t0004 | 0/0 | 5258 | 3 | 0 | 0 | 3 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0004c0005t0001 | 0/0 | 5258 | 25 | 6 | 0 | 16 | 0 | 3 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0004c0005t0002 | 0/0 | 5258 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0004c0005t0005 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0004c0005t0015 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0004c0007t0002 | 0/0 | 5258 | 4 | 0 | 3 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0004c0007t0024 | 0/0 | 5258 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0005c0006t0005 | 0/0 | 5258 | 3 | 3 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0005c0006t0009 | 0/0 | 5258 | 5 | 2 | 3 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0006c0008t0004 | 0/0 | 5258 | 3 | 1 | 1 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0006c0008t0018 | 0/0 | 5258 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0007c0009t0004 | 0/0 | 5258 | 3 | 3 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0008c0011t0001 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0008c0011t0005 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0009c0028t0002 | 0/0 | 5258 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0010c0027t0001 | 0/0 | 5258 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0011c0012t0028 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0012c0020t0001 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0013c0024t0014 | 0/0 | 5258 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0014c0016t0003 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0015c0015t0005 | 0/0 | 5258 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0016c0022t0003 | 0/0 | 5258 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
a0017c0025t0002 | 0/0 | 5258 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | copy fasta | chr5 | 149995739 | 150058128 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0003 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0029 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0005g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0006g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0011g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0011g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0011g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0011g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0012g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0012g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0013g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0013g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0021g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0026g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0027g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0001t0029g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0005g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0005g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0005g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0005g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0005g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0005g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0005g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0005g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0005g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0005g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0005g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0005g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0005g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0006g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0006g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0006g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0006g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0006g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0006g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0006g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0008g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0008g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0008g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0008g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0008g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0008g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0019g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0020g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0003t0030g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0017t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0018t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0019t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0021t0006g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0001c0026t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0002 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0007 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0066 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0005g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0005g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0005g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0010g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0010g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0010g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0015g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0016g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0022g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0023g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0002t0025g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0013t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0014t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0002c0023t0014g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0004t0004g0001 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0004t0004g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0004t0004g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0004t0004g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0004t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0004t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0004t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0004t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0004t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0004t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0004t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0004t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0004t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0004t0004g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0004t0004g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0004t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0004t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0004t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0004t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0004t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0004t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0004t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0004t0007g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0004t0007g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0004t0007g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0004t0007g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0004t0007g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0004t0017g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0010t0004g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0003c0010t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0005t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0005t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0005t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0005t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0005t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0005t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0005t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0005t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0005t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0005t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0005t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0005t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0005t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0005t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0005t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0005t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0005t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0005t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0005t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0005t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0005t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0005t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0005t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0005t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0005t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0005t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0005t0015g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0007t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0007t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0007t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0007t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0004c0007t0024g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0005c0006t0005g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0005c0006t0009g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0005c0006t0009g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0005c0006t0009g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0006c0008t0004g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0006c0008t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0006c0008t0018g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0007c0009t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0007c0009t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0007c0009t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0008c0011t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0008c0011t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0009c0028t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0010c0027t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0011c0012t0028g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0012c0020t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0013c0024t0014g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0014c0016t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0015c0015t0005g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0016c0022t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
a0017c0025t0002g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0004 | t0007 | g0136 | EUR | GBR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG00099 | hp2 | a0001 | c0017 | t0003 | g0207 | EUR | GBR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0281 | EUR | GBR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG00140 | hp2 | a0002 | c0002 | t0002 | g0041 | EUR | GBR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG00438 | hp2 | a0002 | c0002 | t0002 | g0056 | EAS | CHS | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG00544 | hp1 | a0003 | c0010 | t0004 | g0130 | EAS | CHS | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0147 | EAS | CHS | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG00597 | hp2 | a0003 | c0004 | t0004 | g0139 | EAS | CHS | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG00609 | hp2 | a0002 | c0002 | t0002 | g0062 | EAS | CHS | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG00639 | hp1 | a0004 | c0007 | t0024 | g0276 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0192 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG00673 | hp1 | a0003 | c0010 | t0004 | g0023 | EAS | CHS | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG00673 | hp2 | a0003 | c0004 | t0004 | g0325 | EAS | CHS | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG00735 | hp1 | a0003 | c0004 | t0007 | g0113 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG00735 | hp2 | a0001 | c0003 | t0005 | g0287 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG00738 | hp1 | a0002 | c0002 | t0002 | g0100 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01069 | hp2 | a0005 | c0006 | t0009 | g0009 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01071 | hp1 | a0005 | c0006 | t0009 | g0009 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01099 | hp1 | a0002 | c0002 | t0002 | g0102 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0225 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01106 | hp1 | a0004 | c0005 | t0002 | g0277 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01106 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0221 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01167 | hp1 | a0001 | c0001 | t0026 | g0208 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01167 | hp2 | a0003 | c0004 | t0007 | g0024 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01168 | hp2 | a0002 | c0002 | t0002 | g0104 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01169 | hp1 | a0003 | c0004 | t0007 | g0024 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01169 | hp2 | a0002 | c0002 | t0002 | g0048 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0224 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0204 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0167 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01243 | hp1 | a0003 | c0004 | t0017 | g0128 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01243 | hp2 | a0001 | c0003 | t0005 | g0140 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01255 | hp1 | a0004 | c0007 | t0002 | g0279 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0226 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0176 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01256 | hp2 | a0002 | c0002 | t0002 | g0017 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01257 | hp2 | a0002 | c0002 | t0002 | g0013 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0017 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01258 | hp2 | a0002 | c0002 | t0002 | g0013 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01346 | hp2 | a0002 | c0014 | t0002 | g0067 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01358 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01361 | hp1 | a0004 | c0007 | t0002 | g0278 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0173 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01433 | hp1 | a0004 | c0007 | t0002 | g0280 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01433 | hp2 | a0003 | c0004 | t0004 | g0001 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01496 | hp1 | a0005 | c0006 | t0009 | g0009 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01496 | hp2 | a0003 | c0004 | t0004 | g0123 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01517 | hp1 | a0002 | c0002 | t0015 | g0103 | EUR | IBS | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0175 | EUR | IBS | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01884 | hp1 | a0005 | c0006 | t0005 | g0008 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01884 | hp2 | a0001 | c0003 | t0006 | g0296 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01891 | hp1 | a0001 | c0003 | t0005 | g0282 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0164 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01928 | hp1 | a0002 | c0002 | t0002 | g0054 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0244 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01934 | hp1 | a0003 | c0004 | t0004 | g0001 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01934 | hp2 | a0001 | c0001 | t0027 | g0174 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01943 | hp1 | a0001 | c0001 | t0012 | g0003 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01943 | hp2 | a0002 | c0002 | t0002 | g0042 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01952 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01952 | hp2 | a0003 | c0004 | t0004 | g0001 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01978 | hp1 | a0003 | c0004 | t0004 | g0001 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01981 | hp1 | a0003 | c0004 | t0004 | g0001 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01981 | hp2 | a0001 | c0003 | t0005 | g0284 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01993 | hp1 | a0003 | c0004 | t0004 | g0116 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG01993 | hp2 | a0003 | c0004 | t0007 | g0137 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02004 | hp1 | a0006 | c0008 | t0004 | g0021 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02027 | hp1 | a0002 | c0002 | t0002 | g0071 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02040 | hp2 | a0006 | c0008 | t0004 | g0126 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02055 | hp1 | a0001 | c0003 | t0020 | g0314 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02055 | hp2 | a0001 | c0003 | t0005 | g0152 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02071 | hp1 | a0002 | c0002 | t0002 | g0039 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02074 | hp1 | a0001 | c0001 | t0005 | g0227 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02074 | hp2 | a0004 | c0005 | t0001 | g0257 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02080 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02083 | hp2 | a0003 | c0004 | t0004 | g0117 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02132 | hp1 | a0003 | c0004 | t0004 | g0124 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02132 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02135 | hp2 | a0004 | c0005 | t0001 | g0261 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02145 | hp1 | a0005 | c0006 | t0009 | g0107 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02145 | hp2 | a0001 | c0003 | t0008 | g0295 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02148 | hp1 | a0003 | c0004 | t0004 | g0122 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0155 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02257 | hp1 | a0001 | c0003 | t0005 | g0239 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0205 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02258 | hp1 | a0004 | c0005 | t0001 | g0249 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02258 | hp2 | a0001 | c0003 | t0005 | g0289 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0156 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02273 | hp2 | a0001 | c0001 | t0013 | g0235 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02280 | hp1 | a0001 | c0003 | t0005 | g0142 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02280 | hp2 | a0007 | c0009 | t0004 | g0132 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02293 | hp1 | a0003 | c0004 | t0004 | g0001 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02293 | hp2 | a0002 | c0002 | t0022 | g0099 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02300 | hp2 | a0003 | c0004 | t0004 | g0001 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02451 | hp2 | a0001 | c0003 | t0008 | g0301 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02572 | hp2 | a0001 | c0003 | t0006 | g0304 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0209 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0181 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02615 | hp1 | a0003 | c0004 | t0004 | g0127 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02615 | hp2 | a0001 | c0001 | t0011 | g0149 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02622 | hp1 | a0001 | c0003 | t0001 | g0322 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02622 | hp2 | a0001 | c0003 | t0005 | g0310 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02630 | hp1 | a0011 | c0012 | t0028 | g0324 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02630 | hp2 | a0001 | c0001 | t0011 | g0012 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02647 | hp2 | a0001 | c0003 | t0005 | g0315 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02683 | hp2 | a0015 | c0015 | t0005 | g0111 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02698 | hp1 | a0002 | c0002 | t0002 | g0055 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0206 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02717 | hp1 | a0005 | c0006 | t0005 | g0008 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02717 | hp2 | a0007 | c0009 | t0004 | g0129 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02735 | hp2 | a0001 | c0026 | t0003 | g0228 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02809 | hp1 | a0004 | c0005 | t0005 | g0253 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02809 | hp2 | a0001 | c0003 | t0005 | g0283 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02818 | hp1 | a0005 | c0006 | t0005 | g0008 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02818 | hp2 | a0001 | c0003 | t0001 | g0323 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02886 | hp1 | a0001 | c0003 | t0030 | g0306 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02886 | hp2 | a0001 | c0001 | t0011 | g0038 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02895 | hp1 | a0001 | c0003 | t0008 | g0291 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02895 | hp2 | a0001 | c0003 | t0001 | g0005 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02896 | hp1 | a0008 | c0011 | t0005 | g0033 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02897 | hp2 | a0001 | c0003 | t0001 | g0005 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02922 | hp1 | a0001 | c0003 | t0005 | g0143 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02922 | hp2 | a0001 | c0003 | t0005 | g0319 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02965 | hp1 | a0001 | c0003 | t0006 | g0303 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02965 | hp2 | a0001 | c0003 | t0005 | g0034 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02970 | hp1 | a0014 | c0016 | t0003 | g0233 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02976 | hp1 | a0001 | c0003 | t0005 | g0005 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02976 | hp2 | a0004 | c0005 | t0001 | g0251 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0214 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03017 | hp2 | a0002 | c0002 | t0002 | g0058 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03041 | hp1 | a0001 | c0003 | t0005 | g0316 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03041 | hp2 | a0001 | c0003 | t0001 | g0313 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03098 | hp1 | a0001 | c0003 | t0001 | g0308 | AFR | MSL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03098 | hp2 | a0001 | c0018 | t0005 | g0141 | AFR | MSL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03130 | hp1 | a0001 | c0003 | t0003 | g0312 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03130 | hp2 | a0001 | c0003 | t0005 | g0153 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03139 | hp1 | a0003 | c0004 | t0004 | g0133 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03139 | hp2 | a0001 | c0003 | t0005 | g0286 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03195 | hp1 | a0001 | c0003 | t0005 | g0034 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03195 | hp2 | a0001 | c0003 | t0005 | g0025 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03209 | hp1 | a0001 | c0003 | t0006 | g0293 | AFR | MSL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03209 | hp2 | a0001 | c0001 | t0021 | g0012 | AFR | MSL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03225 | hp1 | a0001 | c0003 | t0005 | g0318 | AFR | MSL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03225 | hp2 | a0004 | c0005 | t0015 | g0254 | AFR | MSL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03239 | hp2 | a0002 | c0002 | t0023 | g0101 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03453 | hp1 | a0001 | c0003 | t0006 | g0307 | AFR | MSL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03453 | hp2 | a0001 | c0001 | t0006 | g0298 | AFR | MSL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03486 | hp1 | a0001 | c0003 | t0008 | g0305 | AFR | MSL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03486 | hp2 | a0001 | c0021 | t0006 | g0294 | AFR | MSL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0223 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03490 | hp2 | a0002 | c0002 | t0002 | g0052 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03491 | hp2 | a0002 | c0002 | t0002 | g0090 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0051 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03516 | hp1 | a0001 | c0003 | t0003 | g0311 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03516 | hp2 | a0001 | c0019 | t0005 | g0144 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03540 | hp1 | a0007 | c0009 | t0004 | g0131 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03540 | hp2 | a0001 | c0003 | t0005 | g0321 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03579 | hp1 | a0001 | c0003 | t0001 | g0317 | AFR | MSL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03579 | hp2 | a0004 | c0005 | t0001 | g0272 | AFR | MSL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03654 | hp1 | a0004 | c0005 | t0001 | g0262 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03654 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03669 | hp1 | a0006 | c0008 | t0018 | g0125 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03669 | hp2 | a0002 | c0002 | t0002 | g0060 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03704 | hp2 | a0004 | c0007 | t0002 | g0275 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03710 | hp1 | a0004 | c0005 | t0001 | g0256 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03831 | hp2 | a0002 | c0002 | t0002 | g0046 | SAS | BEB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0145 | SAS | BEB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | BEB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0234 | SAS | BEB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03927 | hp2 | a0002 | c0002 | t0003 | g0049 | SAS | BEB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03942 | hp1 | a0002 | c0002 | t0005 | g0057 | SAS | BEB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03942 | hp2 | a0002 | c0002 | t0025 | g0089 | SAS | BEB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0166 | SAS | BEB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG04184 | hp2 | a0002 | c0002 | t0002 | g0091 | SAS | BEB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG04199 | hp1 | a0016 | c0022 | t0003 | g0189 | SAS | STU | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG04199 | hp2 | a0002 | c0002 | t0002 | g0059 | SAS | STU | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG04204 | hp1 | a0004 | c0005 | t0001 | g0268 | SAS | STU | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG04204 | hp2 | a0002 | c0002 | t0003 | g0240 | SAS | STU | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0050 | SAS | STU | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0290 | SAS | STU | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18522 | hp1 | a0004 | c0005 | t0001 | g0250 | AFR | YRI | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18522 | hp2 | a0003 | c0004 | t0004 | g0022 | AFR | YRI | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18612 | hp2 | a0002 | c0002 | t0002 | g0040 | EAS | CHB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18906 | hp1 | a0001 | c0001 | t0011 | g0037 | AFR | YRI | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18906 | hp2 | a0001 | c0003 | t0008 | g0300 | AFR | YRI | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18939 | hp1 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18939 | hp2 | a0002 | c0002 | t0010 | g0092 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18941 | hp2 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18942 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18946 | hp1 | a0004 | c0005 | t0001 | g0260 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18948 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18951 | hp1 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18953 | hp2 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18954 | hp2 | a0002 | c0002 | t0005 | g0047 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18956 | hp1 | a0010 | c0027 | t0001 | g0230 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18956 | hp2 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18957 | hp1 | a0003 | c0004 | t0004 | g0114 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18959 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18961 | hp2 | a0003 | c0004 | t0004 | g0135 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18964 | hp2 | a0003 | c0010 | t0004 | g0023 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18965 | hp1 | a0004 | c0005 | t0001 | g0032 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18965 | hp2 | a0002 | c0002 | t0010 | g0004 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18968 | hp1 | a0004 | c0005 | t0001 | g0267 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18968 | hp2 | a0002 | c0002 | t0010 | g0004 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18969 | hp1 | a0004 | c0005 | t0001 | g0271 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18969 | hp2 | a0002 | c0002 | t0010 | g0004 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18971 | hp1 | a0003 | c0004 | t0004 | g0020 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18971 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18973 | hp1 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18979 | hp1 | a0004 | c0005 | t0001 | g0269 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18982 | hp1 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18982 | hp2 | a0003 | c0004 | t0004 | g0118 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18983 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18984 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18984 | hp2 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18989 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18991 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18992 | hp1 | a0001 | c0001 | t0012 | g0211 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18992 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18995 | hp1 | a0004 | c0005 | t0001 | g0264 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18997 | hp1 | a0003 | c0004 | t0004 | g0119 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18997 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18998 | hp1 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18999 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19000 | hp1 | a0003 | c0004 | t0004 | g0138 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19001 | hp1 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19001 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19003 | hp1 | a0002 | c0002 | t0010 | g0087 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19005 | hp1 | a0004 | c0005 | t0001 | g0259 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19006 | hp2 | a0003 | c0004 | t0004 | g0112 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19007 | hp1 | a0004 | c0005 | t0001 | g0032 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19009 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19011 | hp1 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19011 | hp2 | a0004 | c0005 | t0001 | g0266 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19012 | hp1 | a0003 | c0004 | t0004 | g0121 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19012 | hp2 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | LWK | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19030 | hp2 | a0001 | c0003 | t0019 | g0288 | AFR | LWK | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0190 | AFR | LWK | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | LWK | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19062 | hp2 | a0002 | c0002 | t0002 | g0146 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19063 | hp1 | a0004 | c0005 | t0001 | g0263 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19063 | hp2 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19065 | hp1 | a0003 | c0004 | t0004 | g0010 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19066 | hp1 | a0002 | c0002 | t0002 | g0148 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19066 | hp2 | a0002 | c0013 | t0002 | g0061 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19067 | hp1 | a0002 | c0002 | t0003 | g0077 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19068 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19068 | hp2 | a0003 | c0004 | t0004 | g0020 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19074 | hp1 | a0009 | c0028 | t0002 | g0086 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19076 | hp1 | a0013 | c0024 | t0014 | g0095 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19076 | hp2 | a0004 | c0005 | t0001 | g0274 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19077 | hp2 | a0004 | c0005 | t0001 | g0255 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19078 | hp1 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19079 | hp2 | a0003 | c0004 | t0004 | g0010 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19080 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19084 | hp1 | a0002 | c0002 | t0016 | g0093 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19084 | hp2 | a0003 | c0004 | t0004 | g0010 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19085 | hp1 | a0004 | c0005 | t0001 | g0258 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19086 | hp2 | a0003 | c0004 | t0004 | g0115 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19087 | hp1 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19087 | hp2 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19088 | hp1 | a0001 | c0001 | t0029 | g0027 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19088 | hp2 | a0002 | c0002 | t0005 | g0004 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19089 | hp2 | a0003 | c0004 | t0004 | g0120 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19090 | hp2 | a0004 | c0005 | t0001 | g0265 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19091 | hp1 | a0002 | c0023 | t0014 | g0094 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19240 | hp1 | a0001 | c0003 | t0005 | g0285 | AFR | YRI | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA19240 | hp2 | a0001 | c0003 | t0008 | g0297 | AFR | YRI | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA20129 | hp1 | a0001 | c0003 | t0005 | g0025 | AFR | ASW | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA20129 | hp2 | a0003 | c0004 | t0004 | g0022 | AFR | ASW | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA20752 | hp1 | a0002 | c0002 | t0002 | g0068 | EUR | TSI | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA20752 | hp2 | a0017 | c0025 | t0002 | g0002 | EUR | TSI | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0028 | EUR | TSI | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA20805 | hp2 | a0003 | c0004 | t0007 | g0134 | EUR | TSI | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA20905 | hp1 | a0001 | c0003 | t0006 | g0299 | SAS | GIH | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0248 | SAS | GIH | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02109 | hp2 | a0001 | c0003 | t0005 | g0005 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02486 | hp1 | a0005 | c0006 | t0009 | g0105 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02486 | hp2 | a0004 | c0005 | t0001 | g0270 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02559 | hp1 | a0001 | c0003 | t0001 | g0320 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG02559 | hp2 | a0001 | c0001 | t0013 | g0236 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03471 | hp1 | a0001 | c0003 | t0006 | g0302 | AFR | MSL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG06807 | hp1 | a0004 | c0005 | t0001 | g0252 | AFR | USA | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0154 | AFR | USA | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18955 | hp1 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA20300 | hp1 | a0001 | c0003 | t0001 | g0309 | AFR | USA | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA20300 | hp2 | a0006 | c0008 | t0004 | g0021 | AFR | USA | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA21309 | hp1 | a0012 | c0020 | t0001 | g0292 | AFR | LWK | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
NA21309 | hp2 | a0008 | c0011 | t0001 | g0033 | AFR | LWK | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0029 | REF | REF | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0066 | REF | REF | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:150004859
|
G | A | 1 | a0007 | 3 | HG02280.hp2 HG02717.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.7G>A | p.Ala3Thr | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/20 | 450/5258 | 7/3879 | 3/1292 | chr5 | 150004859 | ||
chr5:150006524
|
G | T | 1 | a0009 | 1 | NA19074.hp1 | missense_variant | MODERATE | c.189G>T | p.Glu63Asp | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/20 | 632/5258 | 189/3879 | 63/1292 | chr5 | 150006524 | ||
chr5:150010226
|
G | T | 1 | a0010 | 1 | NA18956.hp1 | missense_variant | MODERATE | c.428G>T | p.Ser143Ile | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/20 | 871/5258 | 428/3879 | 143/1292 | chr5 | 150010226 | ||
chr5:150010399
|
G | A | 1 | a0011 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.601G>A | p.Val201Ile | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/20 | 1044/5258 | 601/3879 | 201/1292 | chr5 | 150010399 | ||
chr5:150010585
|
G | A | 3 | a0003a0006a0007 | 49 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
missense_variant | MODERATE | c.787G>A | p.Val263Ile | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/20 | 1230/5258 | 787/3879 | 263/1292 | chr5 | 150010585 | ||
chr5:150012282
|
C | T | 1 | a0017 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.838C>T | p.Pro280Ser | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/20 | 1281/5258 | 838/3879 | 280/1292 | chr5 | 150012282 | ||
chr5:150024616
|
G | T | 1 | a0004 | 33 | HG00639.hp1 HG01106.hp1 HG01255.hp1 others(30): Show |
missense_variant | MODERATE | c.1396G>T | p.Val466Leu | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/20 | 1839/5258 | 1396/3879 | 466/1292 | chr5 | 150024616 | ||
chr5:150024631
|
G | A | 1 | a0016 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.1411G>A | p.Glu471Lys | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/20 | 1854/5258 | 1411/3879 | 471/1292 | chr5 | 150024631 | ||
chr5:150024650
|
G | T | 2 | a0008a0012 | 3 | HG02896.hp1 NA21309.hp1 NA21309.hp2 |
missense_variant | MODERATE | c.1430G>T | p.Ser477Ile | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/20 | 1873/5258 | 1430/3879 | 477/1292 | chr5 | 150024650 | ||
chr5:150026708
|
C | T | 13 | a0001a0003a0004others(10): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
missense_variant&splice_region_variant | MODERATE | c.1463C>T | p.Ala488Val | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 8/20 | 1906/5258 | 1463/3879 | 488/1292 | chr5 | 150026708 | ||
chr5:150030756
|
T | A | 1 | a0006 | 4 | HG02004.hp1 HG02040.hp2 HG03669.hp1 others(1): Show |
missense_variant | MODERATE | c.1750T>A | p.Ser584Thr | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/20 | 2193/5258 | 1750/3879 | 584/1292 | chr5 | 150030756 | ||
chr5:150036931
|
G | A | 1 | a0005 | 8 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(5): Show |
missense_variant | MODERATE | c.2279G>A | p.Gly760Glu | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 12/20 | 2722/5258 | 2279/3879 | 760/1292 | chr5 | 150036931 | ||
chr5:150037489
|
A | G | 1 | a0008 | 2 | HG02896.hp1 NA21309.hp2 |
missense_variant | MODERATE | c.2375A>G | p.His792Arg | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/20 | 2818/5258 | 2375/3879 | 792/1292 | chr5 | 150037489 | ||
chr5:150051824
|
C | T | 1 | a0013 | 1 | NA19076.hp1 | missense_variant | MODERATE | c.3511C>T | p.Arg1171Cys | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 3954/5258 | 3511/3879 | 1171/1292 | chr5 | 150051824 | ||
chr5:150051953
|
G | A | 1 | a0015 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.3640G>A | p.Gly1214Ser | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 4083/5258 | 3640/3879 | 1214/1292 | chr5 | 150051953 | ||
chr5:150052176
|
C | G | 1 | a0014 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.3863C>G | p.Ala1288Gly | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 4306/5258 | 3863/3879 | 1288/1292 | chr5 | 150052176 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:150010245
|
A | G | 1 | a0001c0026 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.447A>G | p.Leu149Leu | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/20 | 890/5258 | 447/3879 | 149/1292 | chr5 | 150010245 | ||
chr5:150018655
|
C | T | 1 | a0003c0010 | 3 | HG00544.hp1 HG00673.hp1 NA18964.hp2 |
synonymous_variant | LOW | c.999C>T | p.Cys333Cys | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/20 | 1442/5258 | 999/3879 | 333/1292 | chr5 | 150018655 | ||
chr5:150024411
|
A | G | 2 | a0002c0023a0013c0024 | 2 | NA19076.hp1 NA19091.hp1 |
synonymous_variant | LOW | c.1191A>G | p.Val397Val | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/20 | 1634/5258 | 1191/3879 | 397/1292 | chr5 | 150024411 | ||
chr5:150024483
|
C | T | 1 | a0016c0022 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.1263C>T | p.Ser421Ser | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/20 | 1706/5258 | 1263/3879 | 421/1292 | chr5 | 150024483 | ||
chr5:150024486
|
T | C | 1 | a0002c0013 | 1 | NA19066.hp2 | synonymous_variant | LOW | c.1266T>C | p.Asp422Asp | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/20 | 1709/5258 | 1266/3879 | 422/1292 | chr5 | 150024486 | ||
chr5:150024630
|
C | T | 1 | a0001c0021 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.1410C>T | p.Ser470Ser | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/20 | 1853/5258 | 1410/3879 | 470/1292 | chr5 | 150024630 | ||
chr5:150026793
|
C | T | 1 | a0001c0019 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.1548C>T | p.Pro516Pro | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 8/20 | 1991/5258 | 1548/3879 | 516/1292 | chr5 | 150026793 | ||
chr5:150026850
|
G | T | 1 | a0004c0007 | 5 | HG00639.hp1 HG01255.hp1 HG01361.hp1 others(2): Show |
synonymous_variant | LOW | c.1605G>T | p.Leu535Leu | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 8/20 | 2048/5258 | 1605/3879 | 535/1292 | chr5 | 150026850 | ||
chr5:150036887
|
G | A | 1 | a0015c0015 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.2235G>A | p.Pro745Pro | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 12/20 | 2678/5258 | 2235/3879 | 745/1292 | chr5 | 150036887 | ||
chr5:150041939
|
A | G | 10 | a0001c0003a0001c0018a0001c0019others(7): Show | 106 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(103): Show |
synonymous_variant | LOW | c.2700A>G | p.Glu900Glu | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/20 | 3143/5258 | 2700/3879 | 900/1292 | chr5 | 150041939 | ||
chr5:150048640
|
A | G | 1 | a0015c0015 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.3156A>G | p.Pro1052Pro | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/20 | 3599/5258 | 3156/3879 | 1052/1292 | chr5 | 150048640 | ||
chr5:150051835
|
T | C | 1 | a0001c0018 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.3522T>C | p.His1174His | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 3965/5258 | 3522/3879 | 1174/1292 | chr5 | 150051835 | ||
chr5:150052141
|
A | G | 1 | a0001c0017 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.3828A>G | p.Thr1276Thr | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 4271/5258 | 3828/3879 | 1276/1292 | chr5 | 150052141 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:150000832
|
T | G | 1 | a0002c0002t0016 | 1 | NA19084.hp1 | 5_prime_UTR_variant | MODIFIER | c.-350T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/20 | 4021 | chr5 | 150000832 | |||||
chr5:150000902
|
C | T | 5 | a0001c0001t0006a0001c0003t0006a0001c0003t0008others(2): Show | 16 | HG01884.hp2 HG02145.hp2 HG02451.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-280C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/20 | 3951 | chr5 | 150000902 | |||||
chr5:150000930
|
G | A | 7 | a0003c0004t0004a0003c0004t0007a0003c0004t0017others(4): Show | 49 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
5_prime_UTR_variant | MODIFIER | c.-252G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/20 | 3923 | chr5 | 150000930 | |||||
chr5:150000990
|
G | T | 1 | a0001c0001t0029 | 1 | NA19088.hp1 | 5_prime_UTR_variant | MODIFIER | c.-192G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/20 | 3863 | chr5 | 150000990 | |||||
chr5:150052206
|
A | G | 1 | a0002c0002t0010 | 5 | NA18939.hp2 NA18965.hp2 NA18968.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*14A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 14 | chr5 | 150052206 | |||||
chr5:150052240
|
G | A | 3 | a0001c0003t0019a0001c0003t0020a0003c0004t0017 | 3 | HG01243.hp1 HG02055.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*48G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 48 | chr5 | 150052240 | |||||
chr5:150052367
|
T | C | 3 | a0001c0001t0011a0001c0001t0021a0001c0003t0030 | 6 | HG02615.hp2 HG02630.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*175T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 175 | chr5 | 150052367 | |||||
chr5:150052374
|
C | T | 1 | a0005c0006t0009 | 5 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*182C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 182 | chr5 | 150052374 | |||||
chr5:150052445
|
G | A | 1 | a0001c0001t0021 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*253G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 253 | chr5 | 150052445 | |||||
chr5:150052476
|
C | G | 51 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(48): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
3_prime_UTR_variant | MODIFIER | c.*284C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 284 | chr5 | 150052476 | |||||
chr5:150052477
|
G | A | 13 | a0001c0001t0003a0001c0001t0012a0001c0001t0013others(10): Show | 60 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*285G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 285 | chr5 | 150052477 | |||||
chr5:150052504
|
G | T | 39 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(36): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
3_prime_UTR_variant | MODIFIER | c.*312G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 312 | chr5 | 150052504 | |||||
chr5:150052571
|
C | T | 1 | a0011c0012t0028 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*379C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 379 | chr5 | 150052571 | |||||
chr5:150052598
|
C | G | 1 | a0004c0007t0024 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*406C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 406 | chr5 | 150052598 | |||||
chr5:150052701
|
T | C | 1 | a0001c0001t0013 | 2 | HG02273.hp2 HG02559.hp2 |
3_prime_UTR_variant | MODIFIER | c.*509T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 509 | chr5 | 150052701 | |||||
chr5:150052746
|
C | T | 1 | a0001c0001t0026 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*554C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 554 | chr5 | 150052746 | |||||
chr5:150052894
|
G | A | 1 | a0002c0002t0022 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*702G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 702 | chr5 | 150052894 | |||||
chr5:150053029
|
T | C | 2 | a0002c0023t0014a0013c0024t0014 | 2 | NA19076.hp1 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*837T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 837 | chr5 | 150053029 | |||||
chr5:150053050
|
A | G | 4 | a0002c0002t0015a0002c0002t0023a0003c0004t0007others(1): Show | 9 | HG00099.hp1 HG00735.hp1 HG01167.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*858A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 858 | chr5 | 150053050 | |||||
chr5:150053100
|
C | G | 1 | a0001c0001t0027 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*908C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 908 | chr5 | 150053100 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:150001269
|
A | G | 1 | a0003c0004t0004g0325 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-3+90A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150001269 | ||||||
chr5:150001448
|
A | G | 1 | a0011c0012t0028g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-3+269A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150001448 | ||||||
chr5:150001685
|
G | T | 35 | a0001c0001t0006g0298a0001c0003t0001g0005a0001c0003t0001g0308others(32): Show | 37 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(34): Show |
intron_variant | MODIFIER | c.-3+506G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150001685 | ||||||
chr5:150001709
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-3+530T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150001709 | ||||||
chr5:150001845
|
C | T | 1 | a0001c0001t0003g0290 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-3+666C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150001845 | ||||||
chr5:150001856
|
A | T | 14 | a0001c0003t0001g0313a0001c0003t0001g0317a0001c0003t0001g0320others(11): Show | 14 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.-3+677A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150001856 | ||||||
chr5:150002026
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-3+847T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150002026 | ||||||
chr5:150002030
|
C | G | 9 | a0001c0003t0005g0034a0001c0003t0005g0282a0001c0003t0005g0283others(6): Show | 10 | HG00735.hp2 HG01891.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.-3+851C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150002030 | ||||||
chr5:150002259
|
T | C | 4 | a0001c0001t0011g0012a0001c0001t0011g0037a0001c0001t0011g0038others(1): Show | 4 | HG02630.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+1080T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150002259 | ||||||
chr5:150002372
|
G | T | 1 | a0001c0001t0003g0281 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3+1193G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150002372 | ||||||
chr5:150002375
|
T | A | 3 | a0001c0003t0005g0282a0001c0003t0005g0283a0001c0003t0005g0284 | 3 | HG01891.hp1 HG01981.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-3+1196T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150002375 | ||||||
chr5:150002389
|
A | C | 145 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(142): Show | 155 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.-3+1210A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150002389 | ||||||
chr5:150002430
|
A | C | 14 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0011g0149others(11): Show | 15 | HG00735.hp2 HG01891.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.-3+1251A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150002430 | ||||||
chr5:150002550
|
C | T | 1 | a0011c0012t0028g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-3+1371C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150002550 | ||||||
chr5:150002845
|
G | C | 110 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(107): Show | 119 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.-3+1666G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150002845 | ||||||
chr5:150002954
|
A | G | 4 | a0002c0002t0002g0145a0002c0002t0002g0146a0002c0002t0002g0147others(1): Show | 4 | HG00597.hp1 HG03834.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+1775A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150002954 | ||||||
chr5:150003170
|
T | G | 1 | a0002c0002t0002g0039 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-2-1681T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150003170 | ||||||
chr5:150003268
|
C | A | 3 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0156 | 3 | HG02148.hp2 HG02273.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-2-1583C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150003268 | ||||||
chr5:150003349
|
G | C | 3 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0011g0149 | 3 | HG02109.hp1 HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-2-1502G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150003349 | ||||||
chr5:150003482
|
C | T | 4 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(1): Show | 6 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-1369C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150003482 | ||||||
chr5:150003578
|
C | G | 6 | a0001c0003t0005g0025a0001c0003t0005g0140a0001c0003t0005g0142others(3): Show | 7 | HG01243.hp2 HG02280.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2-1273C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150003578 | ||||||
chr5:150003619
|
T | C | 1 | a0002c0002t0002g0040 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-2-1232T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150003619 | ||||||
chr5:150003634
|
A | AT | 145 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(142): Show | 155 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.-2-1208dupT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 150003634 | |||||
chr5:150003678
|
A | T | 238 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(235): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-2-1173A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150003678 | ||||||
chr5:150003687
|
T | C | 1 | a0015c0015t0005g0111 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-2-1164T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150003687 | ||||||
chr5:150003743
|
C | T | 4 | a0002c0002t0001g0110a0002c0002t0002g0019a0002c0002t0002g0108others(1): Show | 5 | NA18941.hp1 NA18989.hp1 NA19078.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-1108C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150003743 | ||||||
chr5:150003748
|
G | A | 6 | a0004c0005t0001g0249a0004c0005t0001g0250a0004c0005t0001g0251others(3): Show | 6 | HG02258.hp1 HG02809.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-1103G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150003748 | ||||||
chr5:150003816
|
C | T | 35 | a0001c0001t0006g0298a0001c0003t0001g0005a0001c0003t0001g0308others(32): Show | 37 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(34): Show |
intron_variant | MODIFIER | c.-2-1035C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150003816 | ||||||
chr5:150003893
|
G | A | 2 | a0002c0002t0002g0041a0002c0002t0002g0042 | 2 | HG00140.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.-2-958G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150003893 | ||||||
chr5:150003948
|
AAAAAAC | A | 5 | a0001c0001t0001g0043a0001c0001t0011g0012a0001c0001t0011g0037others(2): Show | 5 | HG02630.hp2 HG02886.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-891_-2-886delCA others(4): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 150003948 | |||||
chr5:150003953
|
ACAAAAAC others(8): Show |
A | 1 | a0001c0001t0003g0248 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-2-887_-2-873delAA others(13): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 150003953 | |||||
chr5:150003977
|
A | T | 6 | a0001c0001t0001g0018a0001c0001t0001g0106a0005c0006t0005g0008others(3): Show | 11 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2-874A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150003977 | ||||||
chr5:150003993
|
A | G | 6 | a0004c0005t0002g0277a0004c0007t0002g0275a0004c0007t0002g0278others(3): Show | 6 | HG00639.hp1 HG01106.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-858A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150003993 | ||||||
chr5:150004011
|
CT | C | 10 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0003t0008g0291others(7): Show | 10 | HG01169.hp2 HG02132.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2-827delT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 150004011 | |||||
chr5:150004137
|
G | A | 1 | a0001c0001t0003g0159 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-2-714G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150004137 | ||||||
chr5:150004213
|
A | G | 56 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0011g0149others(53): Show | 71 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.-2-638A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150004213 | ||||||
chr5:150004308
|
A | C | 91 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0006g0298others(88): Show | 108 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.-2-543A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150004308 | ||||||
chr5:150004391
|
G | C | 249 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0018others(246): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.-2-460G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150004391 | ||||||
chr5:150004413
|
A | G | 56 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0011g0149others(53): Show | 71 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.-2-438A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150004413 | ||||||
chr5:150004565
|
C | T | 5 | a0001c0001t0001g0043a0001c0001t0011g0012a0001c0001t0011g0037others(2): Show | 5 | HG02630.hp2 HG02886.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-286C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150004565 | ||||||
chr5:150004590
|
C | T | 1 | a0015c0015t0005g0111 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-2-261C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150004590 | ||||||
chr5:150004591
|
G | A | 5 | a0001c0001t0001g0043a0001c0001t0011g0012a0001c0001t0011g0037others(2): Show | 5 | HG02630.hp2 HG02886.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-260G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150004591 | ||||||
chr5:150004642
|
T | C | 1 | a0003c0004t0004g0112 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-2-209T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150004642 | ||||||
chr5:150004648
|
G | T | 3 | a0001c0003t0006g0307a0001c0003t0008g0291a0001c0003t0030g0306 | 3 | HG02886.hp1 HG02895.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-2-203G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150004648 | ||||||
chr5:150005047
|
C | T | 10 | a0002c0002t0002g0002a0002c0002t0002g0017a0002c0002t0002g0048others(7): Show | 14 | HG00738.hp1 HG01099.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.137+58C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005047 | ||||||
chr5:150005112
|
G | A | 36 | a0003c0004t0004g0001a0003c0004t0004g0010a0003c0004t0004g0020others(33): Show | 49 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.137+123G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005112 | ||||||
chr5:150005117
|
A | G | 249 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0018others(246): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.137+128A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005117 | ||||||
chr5:150005162
|
C | T | 10 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0035others(7): Show | 12 | HG01346.hp1 HG01358.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.137+173C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005162 | ||||||
chr5:150005254
|
A | G | 1 | a0001c0001t0003g0241 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.137+265A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005254 | ||||||
chr5:150005332
|
G | T | 53 | a0001c0003t0005g0025a0001c0003t0005g0034a0001c0003t0005g0140others(50): Show | 68 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.137+343G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005332 | ||||||
chr5:150005381
|
C | T | 32 | a0001c0001t0006g0298a0001c0003t0001g0005a0001c0003t0001g0308others(29): Show | 34 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.137+392C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005381 | ||||||
chr5:150005468
|
G | A | 53 | a0001c0003t0005g0025a0001c0003t0005g0034a0001c0003t0005g0140others(50): Show | 68 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.137+479G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005468 | ||||||
chr5:150005539
|
C | T | 20 | a0001c0001t0006g0298a0001c0003t0001g0005a0001c0003t0001g0308others(17): Show | 22 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.137+550C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005539 | ||||||
chr5:150005540
|
G | A | 1 | a0003c0004t0004g0325 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.137+551G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005540 | ||||||
chr5:150005598
|
C | CAA | 16 | a0001c0003t0005g0025a0001c0003t0005g0034a0001c0003t0005g0140others(13): Show | 18 | HG00735.hp2 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.137+624_137+625dup others(2): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 150005598 | |||||
chr5:150005598
|
C | CAAA | 35 | a0001c0003t0005g0285a0003c0004t0004g0001a0003c0004t0004g0010others(32): Show | 48 | HG00099.hp1 HG00544.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.137+623_137+625dup others(3): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 150005598 | |||||
chr5:150005610
|
A | G | 40 | a0002c0002t0001g0016a0002c0002t0001g0081a0002c0002t0002g0007others(37): Show | 46 | HG00597.hp1 HG01106.hp2 HG01952.hp1 others(43): Show |
intron_variant | MODIFIER | c.137+621A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005610 | ||||||
chr5:150005634
|
A | C | 248 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0018others(245): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.137+645A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005634 | ||||||
chr5:150005660
|
A | C | 1 | a0004c0005t0001g0274 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.137+671A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005660 | ||||||
chr5:150005831
|
C | T | 53 | a0001c0003t0005g0025a0001c0003t0005g0034a0001c0003t0005g0140others(50): Show | 68 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.138-642C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005831 | ||||||
chr5:150005862
|
G | A | 53 | a0001c0003t0005g0025a0001c0003t0005g0034a0001c0003t0005g0140others(50): Show | 68 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.138-611G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005862 | ||||||
chr5:150005944
|
A | G | 1 | a0001c0003t0008g0305 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.138-529A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005944 | ||||||
chr5:150006309
|
T | G | 36 | a0003c0004t0004g0001a0003c0004t0004g0010a0003c0004t0004g0020others(33): Show | 49 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.138-164T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150006309 | ||||||
chr5:150006353
|
C | T | 2 | a0001c0001t0001g0238a0001c0003t0005g0239 | 2 | HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.138-120C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150006353 | ||||||
chr5:150006751
|
G | C | 90 | a0001c0001t0006g0298a0001c0003t0001g0005a0001c0003t0001g0308others(87): Show | 107 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.312+104G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150006751 | ||||||
chr5:150006759
|
G | A | 2 | a0001c0001t0001g0160a0004c0005t0001g0249 | 2 | HG02129.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.312+112G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150006759 | ||||||
chr5:150006843
|
C | T | 3 | a0002c0002t0002g0096a0002c0002t0002g0097a0002c0002t0002g0098 | 3 | NA18950.hp2 NA18982.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.312+196C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150006843 | ||||||
chr5:150006913
|
T | A | 1 | a0002c0002t0002g0072 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.312+266T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150006913 | ||||||
chr5:150007153
|
G | A | 247 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0018others(244): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.312+506G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150007153 | ||||||
chr5:150007223
|
C | T | 1 | a0001c0001t0001g0237 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.312+576C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150007223 | ||||||
chr5:150007276
|
C | T | 1 | a0001c0003t0005g0289 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.312+629C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150007276 | ||||||
chr5:150007355
|
C | G | 1 | a0001c0001t0003g0156 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.312+708C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150007355 | ||||||
chr5:150007446
|
A | C | 2 | a0005c0006t0009g0009a0005c0006t0009g0107 | 4 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.312+799A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150007446 | ||||||
chr5:150007731
|
T | C | 1 | a0001c0001t0003g0281 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.312+1084T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150007731 | ||||||
chr5:150007926
|
A | G | 3 | a0001c0003t0006g0302a0001c0003t0006g0303a0001c0003t0006g0304 | 3 | HG02572.hp2 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.312+1279A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150007926 | ||||||
chr5:150007963
|
G | A | 1 | a0003c0004t0007g0113 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.312+1316G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150007963 | ||||||
chr5:150007980
|
C | A | 9 | a0002c0002t0002g0007a0002c0002t0002g0015a0002c0002t0002g0040others(6): Show | 12 | HG01106.hp2 HG01952.hp1 NA18612.hp2 others(9): Show |
intron_variant | MODIFIER | c.312+1333C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150007980 | ||||||
chr5:150008054
|
T | TTC | 6 | a0001c0001t0011g0038a0001c0001t0011g0149a0001c0003t0005g0239others(3): Show | 6 | HG00735.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.312+1408_312+1409d others(4): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008054 | |||||
chr5:150008055
|
T | TCA | 12 | a0002c0002t0002g0015a0002c0002t0002g0042a0002c0002t0002g0048others(9): Show | 13 | HG01168.hp2 HG01169.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.312+1451_312+1452d others(4): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008055 | |||||
chr5:150008055
|
T | TCTCA | 11 | a0001c0001t0001g0018a0001c0001t0001g0151a0001c0001t0011g0012others(8): Show | 14 | HG01243.hp2 HG01993.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.312+1409_312+1410i others(6): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008055 | |||||
chr5:150008055
|
T | TCTCACA | 12 | a0003c0004t0004g0133a0003c0004t0004g0135a0003c0004t0007g0024others(9): Show | 14 | HG00099.hp1 HG00544.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.312+1409_312+1410i others(8): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008055 | |||||
chr5:150008055
|
T | TCTCACAC others(1): Show |
3 | a0001c0001t0001g0150a0003c0004t0004g0022a0003c0004t0017g0128 | 4 | HG01243.hp1 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.312+1409_312+1410i others(10): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008055 | |||||
chr5:150008055
|
T | TCTCACAC others(3): Show |
1 | a0003c0004t0004g0127 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.312+1409_312+1410i others(12): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008055 | |||||
chr5:150008055
|
T | TCTCACAC others(5): Show |
1 | a0001c0001t0001g0043 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.312+1409_312+1410i others(14): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008055 | |||||
chr5:150008055
|
TCA | T | 122 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0030others(119): Show | 134 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.312+1451_312+1452d others(4): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008055 | |||||
chr5:150008055
|
TCACA | T | 27 | a0001c0001t0001g0027a0001c0001t0001g0170a0001c0001t0001g0171others(24): Show | 27 | HG00597.hp1 HG01256.hp1 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.312+1449_312+1452d others(6): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008055 | |||||
chr5:150008055
|
TCACACA | T | 11 | a0001c0001t0001g0026a0001c0001t0001g0165a0001c0001t0001g0168others(8): Show | 12 | HG01192.hp2 HG02074.hp2 HG03471.hp1 others(9): Show |
intron_variant | MODIFIER | c.312+1447_312+1452d others(8): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008055 | |||||
chr5:150008055
|
TCACACAC others(3): Show |
T | 1 | a0002c0002t0002g0078 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.312+1443_312+1452d others(12): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008055 | |||||
chr5:150008055
|
TCACACAC others(7): Show |
T | 4 | a0001c0001t0001g0162a0001c0001t0002g0161a0001c0001t0002g0163others(1): Show | 4 | HG01071.hp2 HG01891.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.312+1439_312+1452d others(16): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008055 | |||||
chr5:150008057
|
A | T | 22 | a0001c0001t0013g0236a0001c0003t0005g0142a0001c0003t0005g0143others(19): Show | 22 | HG00639.hp1 HG01106.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.312+1410A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008057 | ||||||
chr5:150008059
|
A | T | 38 | a0001c0001t0003g0234a0001c0001t0006g0298a0001c0001t0013g0235others(35): Show | 39 | HG01884.hp2 HG02135.hp2 HG02145.hp2 others(36): Show |
intron_variant | MODIFIER | c.312+1412A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008059 | ||||||
chr5:150008061
|
A | T | 10 | a0001c0003t0001g0313a0001c0003t0006g0293a0001c0003t0006g0303others(7): Show | 10 | HG02055.hp1 HG02886.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.312+1414A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008061 | ||||||
chr5:150008063
|
A | T | 4 | a0001c0003t0006g0302a0004c0005t0001g0250a0004c0005t0001g0256others(1): Show | 4 | HG02074.hp2 HG03471.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.312+1416A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008063 | ||||||
chr5:150008094
|
C | CACACAT | 9 | a0003c0004t0004g0020a0003c0004t0004g0116a0003c0004t0004g0117others(6): Show | 10 | HG00597.hp2 HG00673.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.312+1452_312+1453i others(8): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008094 | |||||
chr5:150008094
|
C | CACAT | 9 | a0003c0004t0004g0001a0003c0004t0004g0010a0003c0004t0004g0112others(6): Show | 18 | HG01433.hp2 HG01496.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.312+1450_312+1451i others(6): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008094 | |||||
chr5:150008094
|
C | T | 52 | a0001c0001t0001g0043a0001c0001t0001g0150a0001c0001t0001g0151others(49): Show | 57 | HG00099.hp1 HG00544.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.312+1447C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008094 | ||||||
chr5:150008099
|
A | AC | 3 | a0002c0002t0002g0070a0002c0002t0002g0071a0013c0024t0014g0095 | 3 | HG02027.hp1 NA18998.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.312+1452_312+1453i others(3): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008099 | ||||||
chr5:150008250
|
A | C | 4 | a0005c0006t0005g0008a0005c0006t0009g0009a0005c0006t0009g0105others(1): Show | 8 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.312+1603A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008250 | ||||||
chr5:150008254
|
A | T | 2 | a0001c0001t0003g0224a0014c0016t0003g0233 | 2 | HG01175.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.312+1607A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008254 | ||||||
chr5:150008290
|
A | AGTTCTT | 4 | a0005c0006t0005g0008a0005c0006t0009g0009a0005c0006t0009g0105others(1): Show | 8 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.312+1644_312+1645i others(8): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008290 | |||||
chr5:150008292
|
G | A | 1 | a0001c0001t0011g0149 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.312+1645G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008292 | ||||||
chr5:150008295
|
A | C | 4 | a0005c0006t0005g0008a0005c0006t0009g0009a0005c0006t0009g0105others(1): Show | 8 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.312+1648A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008295 | ||||||
chr5:150008296
|
G | T | 4 | a0005c0006t0005g0008a0005c0006t0009g0009a0005c0006t0009g0105others(1): Show | 8 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.312+1649G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008296 | ||||||
chr5:150008297
|
T | TGGCTA | 4 | a0005c0006t0005g0008a0005c0006t0009g0009a0005c0006t0009g0105others(1): Show | 8 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.312+1650_312+1651i others(7): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008297 | ||||||
chr5:150008777
|
C | T | 53 | a0001c0003t0005g0025a0001c0003t0005g0034a0001c0003t0005g0140others(50): Show | 68 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.313-1334C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008777 | ||||||
chr5:150008905
|
G | A | 1 | a0003c0004t0007g0137 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.313-1206G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008905 | ||||||
chr5:150008962
|
C | T | 1 | a0002c0002t0002g0223 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.313-1149C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008962 | ||||||
chr5:150009061
|
T | G | 145 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(142): Show | 155 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.313-1050T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150009061 | ||||||
chr5:150009301
|
T | C | 36 | a0003c0004t0004g0001a0003c0004t0004g0010a0003c0004t0004g0020others(33): Show | 49 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.313-810T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150009301 | ||||||
chr5:150009370
|
A | T | 1 | a0004c0005t0001g0270 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.313-741A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150009370 | ||||||
chr5:150009641
|
T | C | 3 | a0001c0001t0001g0162a0001c0001t0002g0161a0001c0001t0002g0163 | 3 | HG01071.hp2 HG02683.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.313-470T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150009641 | ||||||
chr5:150009777
|
G | A | 1 | a0002c0002t0002g0053 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.313-334G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150009777 | ||||||
chr5:150009814
|
T | G | 4 | a0003c0004t0004g0001a0003c0004t0004g0116a0003c0004t0004g0122others(1): Show | 10 | HG01433.hp2 HG01496.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.313-297T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150009814 | ||||||
chr5:150009902
|
C | T | 144 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(141): Show | 154 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.313-209C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150009902 | ||||||
chr5:150010010
|
A | G | 36 | a0003c0004t0004g0001a0003c0004t0004g0010a0003c0004t0004g0020others(33): Show | 49 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.313-101A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150010010 | ||||||
chr5:150010084
|
C | T | 15 | a0001c0003t0001g0313a0001c0003t0001g0317a0001c0003t0001g0320others(12): Show | 15 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.313-27C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150010084 | ||||||
chr5:150010109
|
A | C | 1 | a0001c0001t0003g0159 | 1 | NA18955.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.313-2A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150010109 | ||||||
chr5:150010659
|
G | C | 9 | a0001c0003t0005g0034a0001c0003t0005g0282a0001c0003t0005g0283others(6): Show | 10 | HG00735.hp2 HG01891.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.810+51G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150010659 | ||||||
chr5:150010899
|
C | G | 1 | a0001c0001t0001g0222 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.810+291C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150010899 | ||||||
chr5:150010906
|
A | G | 1 | a0003c0004t0004g0123 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.810+298A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150010906 | ||||||
chr5:150011109
|
C | G | 6 | a0001c0003t0005g0025a0001c0003t0005g0140a0001c0003t0005g0142others(3): Show | 7 | HG01243.hp2 HG02280.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.810+501C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011109 | ||||||
chr5:150011244
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.810+636G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011244 | ||||||
chr5:150011245
|
G | A | 3 | a0005c0006t0009g0009a0005c0006t0009g0105a0005c0006t0009g0107 | 5 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.810+637G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011245 | ||||||
chr5:150011337
|
G | A | 1 | a0002c0002t0002g0100 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.810+729G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011337 | ||||||
chr5:150011384
|
T | C | 249 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0018others(246): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.810+776T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011384 | ||||||
chr5:150011459
|
T | C | 1 | a0001c0001t0003g0179 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.811-796T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011459 | ||||||
chr5:150011594
|
T | A | 1 | a0001c0003t0001g0317 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.811-661T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011594 | ||||||
chr5:150011594
|
T | G | 319 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0018others(316): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.811-661T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011594 | ||||||
chr5:150011603
|
G | GT | 45 | a0001c0001t0006g0298a0001c0003t0001g0005a0001c0003t0001g0309others(42): Show | 48 | HG00735.hp2 HG01884.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.811-652_811-651ins others(1): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011603 | ||||||
chr5:150011604
|
G | GT | 51 | a0001c0001t0001g0158a0001c0001t0001g0178a0001c0001t0001g0220others(48): Show | 52 | HG00140.hp2 HG00621.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.811-634dupT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr5 | 150011604 | |||||
chr5:150011604
|
G | T | 53 | a0001c0001t0006g0298a0001c0003t0001g0005a0001c0003t0001g0308others(50): Show | 57 | HG00735.hp2 HG01243.hp2 HG01884.hp2 others(54): Show |
intron_variant | MODIFIER | c.811-651G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011604 | ||||||
chr5:150011623
|
A | T | 1 | a0001c0001t0001g0238 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.811-632A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011623 | ||||||
chr5:150011667
|
C | A | 1 | a0001c0001t0001g0180 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.811-588C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011667 | ||||||
chr5:150011814
|
G | A | 17 | a0001c0003t0005g0025a0001c0003t0005g0034a0001c0003t0005g0140others(14): Show | 19 | HG00735.hp2 HG01243.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.811-441G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011814 | ||||||
chr5:150011822
|
G | A | 1 | a0002c0002t0002g0223 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.811-433G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011822 | ||||||
chr5:150011844
|
T | A | 2 | a0002c0002t0002g0013a0002c0002t0002g0054 | 3 | HG01257.hp2 HG01258.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.811-411T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011844 | ||||||
chr5:150011907
|
C | T | 1 | a0002c0002t0001g0110 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.811-348C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011907 | ||||||
chr5:150011913
|
C | T | 1 | a0001c0001t0003g0221 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.811-342C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011913 | ||||||
chr5:150012042
|
T | G | 1 | a0011c0012t0028g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.811-213T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150012042 | ||||||
chr5:150012066
|
C | T | 3 | a0001c0003t0005g0025a0001c0003t0005g0140a0001c0018t0005g0141 | 4 | HG01243.hp2 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.811-189C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150012066 | ||||||
chr5:150012240
|
C | T | 1 | a0001c0001t0001g0220 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.811-15C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150012240 | ||||||
chr5:150012494
|
G | C | 1 | a0002c0002t0003g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.909+141G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150012494 | ||||||
chr5:150012580
|
A | G | 1 | a0001c0001t0001g0231 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.909+227A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150012580 | ||||||
chr5:150012655
|
A | G | 1 | a0001c0001t0002g0218 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.909+302A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150012655 | ||||||
chr5:150012743
|
C | T | 2 | a0004c0005t0001g0256a0004c0005t0001g0257 | 2 | HG02074.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.909+390C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150012743 | ||||||
chr5:150012762
|
C | T | 6 | a0001c0001t0001g0018a0001c0001t0001g0106a0005c0006t0005g0008others(3): Show | 11 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.909+409C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150012762 | ||||||
chr5:150012814
|
C | T | 144 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(141): Show | 154 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.909+461C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150012814 | ||||||
chr5:150012843
|
T | C | 1 | a0007c0009t0004g0129 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.909+490T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150012843 | ||||||
chr5:150012972
|
T | C | 2 | a0002c0002t0002g0050a0002c0002t0002g0055 | 2 | HG02698.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.909+619T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150012972 | ||||||
chr5:150013353
|
G | C | 6 | a0001c0003t0005g0025a0001c0003t0005g0140a0001c0003t0005g0142others(3): Show | 7 | HG01243.hp2 HG02280.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.909+1000G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150013353 | ||||||
chr5:150013407
|
G | A | 1 | a0001c0003t0005g0282 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.909+1054G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150013407 | ||||||
chr5:150013443
|
G | T | 247 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0018others(244): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.909+1090G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150013443 | ||||||
chr5:150013538
|
A | G | 4 | a0002c0002t0002g0040a0002c0002t0002g0074a0002c0002t0002g0075others(1): Show | 4 | NA18612.hp2 NA18942.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+1185A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150013538 | ||||||
chr5:150013657
|
A | G | 2 | a0001c0001t0001g0169a0001c0001t0001g0217 | 2 | HG00621.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.909+1304A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150013657 | ||||||
chr5:150013756
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0106 | 3 | HG02451.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.909+1403C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150013756 | ||||||
chr5:150013834
|
A | G | 2 | a0001c0003t0001g0323a0001c0003t0005g0316 | 2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.909+1481A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150013834 | ||||||
chr5:150013842
|
A | G | 2 | a0001c0003t0001g0323a0001c0003t0005g0316 | 2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.909+1489A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150013842 | ||||||
chr5:150014061
|
C | A | 1 | a0015c0015t0005g0111 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.909+1708C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150014061 | ||||||
chr5:150014078
|
G | T | 1 | a0003c0004t0004g0121 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.909+1725G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150014078 | ||||||
chr5:150014238
|
A | G | 1 | a0003c0004t0007g0113 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.909+1885A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150014238 | ||||||
chr5:150014331
|
C | T | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | NA18999.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.909+1978C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150014331 | ||||||
chr5:150014559
|
C | G | 1 | a0001c0001t0003g0214 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.909+2206C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150014559 | ||||||
chr5:150014740
|
A | G | 4 | a0001c0001t0001g0213a0001c0001t0003g0210a0001c0001t0003g0212others(1): Show | 4 | NA18991.hp1 NA18992.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+2387A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150014740 | ||||||
chr5:150014848
|
G | A | 1 | a0001c0001t0001g0242 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.909+2495G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150014848 | ||||||
chr5:150014892
|
A | G | 2 | a0001c0001t0003g0175a0001c0001t0003g0176 | 2 | HG01256.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.909+2539A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150014892 | ||||||
chr5:150014910
|
C | T | 1 | a0001c0003t0019g0288 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.909+2557C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150014910 | ||||||
chr5:150014941
|
G | C | 6 | a0001c0001t0001g0018a0001c0001t0001g0106a0005c0006t0005g0008others(3): Show | 11 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.909+2588G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150014941 | ||||||
chr5:150015019
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.909+2666A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015019 | ||||||
chr5:150015023
|
C | T | 1 | a0015c0015t0005g0111 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.909+2670C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015023 | ||||||
chr5:150015095
|
C | G | 2 | a0002c0002t0002g0041a0002c0002t0002g0042 | 2 | HG00140.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.909+2742C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015095 | ||||||
chr5:150015110
|
C | T | 1 | a0004c0005t0001g0271 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.909+2757C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015110 | ||||||
chr5:150015141
|
C | A | 53 | a0001c0003t0005g0025a0001c0003t0005g0034a0001c0003t0005g0140others(50): Show | 68 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.909+2788C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015141 | ||||||
chr5:150015253
|
G | A | 1 | a0004c0005t0001g0260 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.909+2900G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015253 | ||||||
chr5:150015278
|
C | CTTTCT | 17 | a0001c0003t0005g0025a0001c0003t0005g0034a0001c0003t0005g0140others(14): Show | 19 | HG00735.hp2 HG01243.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.909+2944_909+2948d others(7): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr5 | 150015278 | |||||
chr5:150015290
|
T | C | 1 | a0001c0001t0003g0181 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.909+2937T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015290 | ||||||
chr5:150015309
|
A | G | 248 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0018others(245): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.909+2956A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015309 | ||||||
chr5:150015391
|
C | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(139): Show | 152 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.909+3038C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015391 | ||||||
chr5:150015402
|
A | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(139): Show | 152 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.909+3049A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015402 | ||||||
chr5:150015504
|
T | C | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG01109.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.910-3062T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015504 | ||||||
chr5:150015578
|
C | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0106a0011c0012t0028g0324 | 4 | HG02451.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.910-2988C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015578 | ||||||
chr5:150015673
|
T | C | 2 | a0001c0001t0001g0165a0001c0001t0001g0178 | 2 | HG03831.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.910-2893T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015673 | ||||||
chr5:150015691
|
A | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(139): Show | 152 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.910-2875A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015691 | ||||||
chr5:150015797
|
T | C | 1 | a0001c0021t0006g0294 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.910-2769T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015797 | ||||||
chr5:150016048
|
T | A | 1 | a0001c0001t0003g0290 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.910-2518T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150016048 | ||||||
chr5:150016197
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0003g0166 | 3 | HG03491.hp1 HG03492.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.910-2369G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150016197 | ||||||
chr5:150016340
|
C | CA | 7 | a0002c0002t0002g0051a0002c0002t0002g0055a0002c0002t0002g0056others(4): Show | 7 | HG00438.hp2 HG01243.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.910-2205dupA | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr5 | 150016340 | |||||
chr5:150016340
|
CA | C | 126 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(123): Show | 139 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(136): Show |
intron_variant | MODIFIER | c.910-2205delA | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr5 | 150016340 | |||||
chr5:150016340
|
CAA | C | 13 | a0001c0001t0001g0018a0001c0001t0001g0106a0001c0001t0001g0162others(10): Show | 14 | HG00099.hp2 HG01069.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.910-2206_910-2205d others(4): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr5 | 150016340 | |||||
chr5:150016359
|
AAAGG | A | 30 | a0002c0002t0001g0273a0004c0005t0001g0032a0004c0005t0001g0249others(27): Show | 31 | HG00639.hp1 HG01106.hp1 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.910-2205_910-2202d others(6): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr5 | 150016359 | |||||
chr5:150016441
|
T | C | 14 | a0001c0003t0001g0313a0001c0003t0001g0317a0001c0003t0001g0320others(11): Show | 14 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.910-2125T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150016441 | ||||||
chr5:150016503
|
A | G | 9 | a0001c0001t0001g0043a0001c0001t0001g0150a0001c0001t0001g0151others(6): Show | 9 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.910-2063A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150016503 | ||||||
chr5:150016564
|
A | G | 1 | a0001c0003t0008g0305 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.910-2002A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150016564 | ||||||
chr5:150016596
|
C | A | 209 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0018others(206): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.910-1970C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150016596 | ||||||
chr5:150016952
|
A | G | 90 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(87): Show | 107 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.910-1614A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150016952 | ||||||
chr5:150016971
|
T | G | 90 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(87): Show | 107 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.910-1595T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150016971 | ||||||
chr5:150017009
|
G | A | 1 | a0001c0017t0003g0207 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.910-1557G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150017009 | ||||||
chr5:150017083
|
C | T | 90 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(87): Show | 107 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.910-1483C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150017083 | ||||||
chr5:150017541
|
C | G | 36 | a0003c0004t0004g0001a0003c0004t0004g0010a0003c0004t0004g0020others(33): Show | 49 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.910-1025C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150017541 | ||||||
chr5:150017624
|
A | G | 1 | a0001c0001t0001g0216 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.910-942A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150017624 | ||||||
chr5:150017874
|
C | T | 33 | a0002c0002t0001g0273a0004c0005t0001g0032a0004c0005t0001g0249others(30): Show | 34 | HG00639.hp1 HG01106.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.910-692C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150017874 | ||||||
chr5:150017896
|
G | C | 1 | a0002c0002t0001g0081 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.910-670G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150017896 | ||||||
chr5:150018008
|
A | G | 16 | a0002c0002t0001g0006a0002c0002t0001g0110a0002c0002t0002g0006others(13): Show | 18 | HG00438.hp2 HG00609.hp2 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.910-558A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150018008 | ||||||
chr5:150018057
|
G | C | 4 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(1): Show | 6 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.910-509G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150018057 | ||||||
chr5:150018162
|
G | A | 1 | a0001c0001t0003g0221 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.910-404G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150018162 | ||||||
chr5:150018261
|
A | G | 1 | a0001c0003t0006g0303 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.910-305A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150018261 | ||||||
chr5:150018281
|
T | C | 2 | a0004c0005t0001g0258a0004c0005t0001g0260 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.910-285T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150018281 | ||||||
chr5:150018299
|
A | G | 11 | a0001c0001t0001g0180a0001c0001t0001g0231a0001c0001t0002g0209others(8): Show | 11 | HG00099.hp2 HG01069.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.910-267A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150018299 | ||||||
chr5:150018365
|
C | T | 2 | a0003c0004t0007g0024a0003c0004t0007g0136 | 3 | HG00099.hp1 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.910-201C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150018365 | ||||||
chr5:150018396
|
A | C | 1 | a0012c0020t0001g0292 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.910-170A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150018396 | ||||||
chr5:150018917
|
A | G | 107 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(104): Show | 116 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.1041+220A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150018917 | ||||||
chr5:150018992
|
C | T | 36 | a0003c0004t0004g0001a0003c0004t0004g0010a0003c0004t0004g0020others(33): Show | 49 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1041+295C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150018992 | ||||||
chr5:150019026
|
C | T | 1 | a0001c0001t0013g0235 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1041+329C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150019026 | ||||||
chr5:150019048
|
A | C | 1 | a0003c0004t0004g0119 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1041+351A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150019048 | ||||||
chr5:150019058
|
C | T | 1 | a0001c0001t0001g0172 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1041+361C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150019058 | ||||||
chr5:150019272
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1041+575C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150019272 | ||||||
chr5:150019279
|
A | G | 17 | a0001c0003t0005g0025a0001c0003t0005g0034a0001c0003t0005g0140others(14): Show | 19 | HG00735.hp2 HG01243.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1041+582A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150019279 | ||||||
chr5:150019602
|
G | A | 1 | a0015c0015t0005g0111 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1041+905G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150019602 | ||||||
chr5:150019627
|
C | G | 34 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(31): Show | 36 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(33): Show |
intron_variant | MODIFIER | c.1041+930C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150019627 | ||||||
chr5:150019679
|
G | A | 1 | a0004c0007t0024g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1041+982G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150019679 | ||||||
chr5:150019733
|
A | G | 37 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(34): Show | 39 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(36): Show |
intron_variant | MODIFIER | c.1041+1036A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150019733 | ||||||
chr5:150019767
|
G | A | 36 | a0003c0004t0004g0001a0003c0004t0004g0010a0003c0004t0004g0020others(33): Show | 49 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1041+1070G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150019767 | ||||||
chr5:150019780
|
T | A | 2 | a0001c0001t0013g0235a0001c0001t0013g0236 | 2 | HG02273.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1041+1083T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150019780 | ||||||
chr5:150019884
|
T | G | 1 | a0004c0005t0001g0258 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1041+1187T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150019884 | ||||||
chr5:150020094
|
G | A | 1 | a0001c0003t0006g0293 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1041+1397G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150020094 | ||||||
chr5:150020191
|
A | G | 1 | a0001c0003t0001g0309 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1041+1494A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150020191 | ||||||
chr5:150020405
|
G | A | 139 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(136): Show | 149 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.1041+1708G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150020405 | ||||||
chr5:150020497
|
C | G | 1 | a0001c0001t0001g0238 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1041+1800C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150020497 | ||||||
chr5:150020587
|
T | C | 1 | a0003c0004t0007g0137 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1041+1890T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150020587 | ||||||
chr5:150020718
|
C | A | 1 | a0001c0001t0003g0241 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1041+2021C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150020718 | ||||||
chr5:150020746
|
C | CT | 74 | a0001c0001t0001g0018a0001c0001t0001g0106a0001c0001t0001g0222others(71): Show | 82 | HG00621.hp2 HG00639.hp1 HG01069.hp2 others(79): Show |
intron_variant | MODIFIER | c.1041+2065dupT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 150020746 | |||||
chr5:150020746
|
C | CTTT | 31 | a0003c0004t0004g0001a0003c0004t0004g0010a0003c0004t0004g0020others(28): Show | 43 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1041+2063_1041+206 others(7): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 150020746 | |||||
chr5:150020746
|
C | CTTTT | 21 | a0001c0003t0005g0025a0001c0003t0005g0034a0001c0003t0005g0140others(18): Show | 24 | HG00735.hp2 HG01243.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.1041+2062_1041+206 others(8): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 150020746 | |||||
chr5:150020907
|
G | A | 35 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(32): Show | 37 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(34): Show |
intron_variant | MODIFIER | c.1041+2210G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150020907 | ||||||
chr5:150020963
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0106 | 3 | HG02451.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1041+2266G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150020963 | ||||||
chr5:150021025
|
T | C | 1 | a0001c0001t0002g0218 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1041+2328T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150021025 | ||||||
chr5:150021155
|
C | T | 249 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0018others(246): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.1041+2458C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150021155 | ||||||
chr5:150021360
|
A | G | 1 | a0001c0003t0008g0301 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1041+2663A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150021360 | ||||||
chr5:150021472
|
T | C | 1 | a0012c0020t0001g0292 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1041+2775T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150021472 | ||||||
chr5:150021519
|
A | G | 2 | a0008c0011t0001g0033a0008c0011t0005g0033 | 2 | HG02896.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1042-2743A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150021519 | ||||||
chr5:150021618
|
G | A | 1 | a0002c0002t0005g0057 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1042-2644G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150021618 | ||||||
chr5:150021761
|
G | A | 1 | a0001c0001t0003g0173 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1042-2501G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150021761 | ||||||
chr5:150021767
|
A | T | 1 | a0004c0005t0015g0254 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1042-2495A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150021767 | ||||||
chr5:150021968
|
C | G | 1 | a0001c0001t0003g0156 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1042-2294C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150021968 | ||||||
chr5:150022033
|
T | C | 241 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0018others(238): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1042-2229T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150022033 | ||||||
chr5:150022059
|
T | TATG | 90 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(87): Show | 107 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.1042-2201_1042-220 others(7): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 150022059 | |||||
chr5:150022077
|
ATTAT | A | 3 | a0008c0011t0001g0033a0008c0011t0005g0033a0012c0020t0001g0292 | 3 | HG02896.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1042-2182_1042-217 others(8): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 150022077 | |||||
chr5:150022211
|
C | G | 6 | a0001c0003t0005g0025a0001c0003t0005g0140a0001c0003t0005g0142others(3): Show | 7 | HG01243.hp2 HG02280.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1042-2051C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150022211 | ||||||
chr5:150022275
|
C | G | 1 | a0001c0001t0001g0180 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1042-1987C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150022275 | ||||||
chr5:150022348
|
T | C | 1 | a0002c0002t0002g0074 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1042-1914T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150022348 | ||||||
chr5:150022550
|
C | T | 36 | a0003c0004t0004g0001a0003c0004t0004g0010a0003c0004t0004g0020others(33): Show | 49 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1042-1712C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150022550 | ||||||
chr5:150022647
|
G | A | 17 | a0001c0003t0005g0025a0001c0003t0005g0034a0001c0003t0005g0140others(14): Show | 19 | HG00735.hp2 HG01243.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1042-1615G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150022647 | ||||||
chr5:150022817
|
C | CT | 148 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0018others(145): Show | 163 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.1042-1426dupT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 150022817 | |||||
chr5:150022817
|
C | CTT | 12 | a0001c0001t0001g0169a0001c0001t0003g0205a0001c0001t0011g0012others(9): Show | 12 | HG01934.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1042-1427_1042-142 others(6): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 150022817 | |||||
chr5:150022817
|
CT | C | 20 | a0001c0003t0001g0313a0001c0003t0001g0317a0001c0003t0001g0320others(17): Show | 22 | HG01257.hp2 HG01258.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1042-1426delT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 150022817 | |||||
chr5:150022857
|
G | A | 2 | a0001c0003t0006g0304a0001c0021t0006g0294 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1042-1405G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150022857 | ||||||
chr5:150022885
|
C | A | 143 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(140): Show | 153 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1042-1377C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150022885 | ||||||
chr5:150022901
|
C | T | 1 | a0001c0003t0001g0309 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1042-1361C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150022901 | ||||||
chr5:150022927
|
C | T | 1 | a0001c0003t0005g0282 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1042-1335C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150022927 | ||||||
chr5:150022986
|
A | AT | 11 | a0001c0003t0003g0312a0001c0003t0008g0297a0001c0003t0008g0300others(8): Show | 11 | HG02027.hp1 HG02071.hp1 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.1042-1253dupT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 150022986 | |||||
chr5:150022986
|
AT | A | 101 | a0001c0001t0001g0018a0001c0001t0001g0043a0001c0001t0001g0106others(98): Show | 121 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(118): Show |
intron_variant | MODIFIER | c.1042-1253delT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 150022986 | |||||
chr5:150022986
|
ATTT | A | 6 | a0001c0001t0001g0203a0001c0001t0001g0229a0001c0001t0003g0179others(3): Show | 6 | HG00738.hp2 HG01175.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.1042-1255_1042-125 others(7): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 150022986 | |||||
chr5:150022986
|
ATTTT | A | 103 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0027others(100): Show | 111 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1042-1256_1042-125 others(8): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 150022986 | |||||
chr5:150023300
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0237 | 2 | NA18959.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1042-962C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150023300 | ||||||
chr5:150023342
|
A | G | 87 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(84): Show | 104 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.1042-920A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150023342 | ||||||
chr5:150023379
|
A | G | 20 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(17): Show | 22 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1042-883A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150023379 | ||||||
chr5:150023395
|
T | C | 2 | a0002c0023t0014g0094a0013c0024t0014g0095 | 2 | NA19076.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1042-867T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150023395 | ||||||
chr5:150023537
|
C | T | 81 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(78): Show | 97 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.1042-725C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150023537 | ||||||
chr5:150023538
|
G | A | 142 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(139): Show | 152 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.1042-724G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150023538 | ||||||
chr5:150023630
|
G | A | 247 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0018others(244): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.1042-632G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150023630 | ||||||
chr5:150023779
|
T | A | 2 | a0003c0010t0004g0023a0003c0010t0004g0130 | 3 | HG00544.hp1 HG00673.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1042-483T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150023779 | ||||||
chr5:150023965
|
C | A | 231 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(228): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1042-297C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150023965 | ||||||
chr5:150024170
|
A | C | 1 | a0001c0001t0001g0201 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1042-92A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150024170 | ||||||
chr5:150024727
|
G | A | 3 | a0008c0011t0001g0033a0008c0011t0005g0033a0012c0020t0001g0292 | 3 | HG02896.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1460+47G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150024727 | ||||||
chr5:150024817
|
C | T | 1 | a0003c0004t0004g0133 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1460+137C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150024817 | ||||||
chr5:150024916
|
A | G | 3 | a0004c0005t0001g0250a0004c0005t0001g0251a0004c0005t0005g0253 | 3 | HG02809.hp1 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1460+236A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150024916 | ||||||
chr5:150025008
|
T | G | 3 | a0007c0009t0004g0129a0007c0009t0004g0131a0007c0009t0004g0132 | 3 | HG02280.hp2 HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1460+328T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150025008 | ||||||
chr5:150025178
|
G | A | 1 | a0001c0001t0003g0225 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1460+498G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150025178 | ||||||
chr5:150025353
|
A | G | 3 | a0001c0001t0001g0169a0001c0001t0001g0217a0004c0005t0001g0272 | 3 | HG00621.hp1 HG03579.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.1460+673A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150025353 | ||||||
chr5:150025373
|
A | G | 1 | a0015c0015t0005g0111 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1460+693A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150025373 | ||||||
chr5:150025420
|
G | T | 108 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(105): Show | 117 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.1460+740G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150025420 | ||||||
chr5:150025504
|
AT | A | 20 | a0001c0001t0001g0018a0001c0001t0001g0043a0001c0001t0001g0106others(17): Show | 23 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.1460+834delT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr5 | 150025504 | |||||
chr5:150025504
|
ATT | A | 53 | a0001c0003t0005g0025a0001c0003t0005g0034a0001c0003t0005g0140others(50): Show | 68 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.1460+833_1460+834d others(4): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr5 | 150025504 | |||||
chr5:150025630
|
C | CG | 26 | a0001c0001t0001g0018a0001c0001t0001g0106a0001c0003t0001g0005others(23): Show | 33 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.1460+951dupG | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr5 | 150025630 | |||||
chr5:150025730
|
G | A | 1 | a0001c0001t0001g0030 | 2 | HG01346.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1461-976G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150025730 | ||||||
chr5:150025931
|
T | C | 1 | a0004c0005t0001g0261 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1461-775T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150025931 | ||||||
chr5:150026032
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0106 | 3 | HG02451.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1461-674G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150026032 | ||||||
chr5:150026037
|
A | G | 1 | a0001c0001t0001g0178 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1461-669A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150026037 | ||||||
chr5:150026051
|
T | C | 2 | a0002c0002t0005g0057a0004c0005t0001g0252 | 2 | HG03942.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1461-655T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150026051 | ||||||
chr5:150026065
|
T | C | 1 | a0004c0005t0001g0252 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1461-641T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150026065 | ||||||
chr5:150026138
|
C | CT | 67 | a0001c0003t0001g0313a0001c0003t0001g0317a0001c0003t0001g0320others(64): Show | 82 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.1461-561dupT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr5 | 150026138 | |||||
chr5:150026324
|
G | A | 1 | a0001c0003t0005g0239 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1461-382G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150026324 | ||||||
chr5:150026606
|
C | T | 2 | a0008c0011t0001g0033a0008c0011t0005g0033 | 2 | HG02896.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1461-100C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150026606 | ||||||
chr5:150026647
|
G | A | 1 | a0001c0001t0001g0172 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1461-59G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150026647 | ||||||
chr5:150027170
|
G | T | 229 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(226): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1734+53G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150027170 | ||||||
chr5:150027440
|
T | C | 1 | a0001c0001t0003g0214 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1734+323T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150027440 | ||||||
chr5:150027553
|
A | AT | 18 | a0001c0001t0001g0018a0001c0001t0001g0106a0001c0001t0001g0157others(15): Show | 19 | HG00673.hp2 HG01433.hp1 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1734+450dupT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150027553 | |||||
chr5:150027631
|
A | G | 6 | a0001c0001t0001g0018a0001c0001t0001g0106a0005c0006t0005g0008others(3): Show | 11 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.1734+514A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150027631 | ||||||
chr5:150027730
|
G | A | 1 | a0006c0008t0018g0125 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1734+613G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150027730 | ||||||
chr5:150027873
|
A | G | 1 | a0015c0015t0005g0111 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1734+756A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150027873 | ||||||
chr5:150027958
|
A | G | 1 | a0001c0001t0003g0204 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1734+841A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150027958 | ||||||
chr5:150028047
|
C | T | 20 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(17): Show | 22 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1734+930C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028047 | ||||||
chr5:150028213
|
G | C | 1 | a0004c0007t0002g0275 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1734+1096G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028213 | ||||||
chr5:150028354
|
T | G | 1 | a0012c0020t0001g0292 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1734+1237T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028354 | ||||||
chr5:150028408
|
T | TTA | 4 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0003t0030g0306others(1): Show | 4 | HG01106.hp1 HG02886.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.1734+1305_1734+130 others(6): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028408 | |||||
chr5:150028426
|
A | G | 2 | a0003c0010t0004g0023a0003c0010t0004g0130 | 3 | HG00544.hp1 HG00673.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1734+1309A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028426 | ||||||
chr5:150028437
|
T | C | 1 | a0001c0001t0003g0179 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1734+1320T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028437 | ||||||
chr5:150028450
|
A | G | 1 | a0002c0002t0002g0063 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1734+1333A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028450 | ||||||
chr5:150028495
|
ATATG | A | 5 | a0001c0003t0005g0152a0001c0003t0005g0286a0003c0004t0004g0022others(2): Show | 6 | HG01243.hp1 HG02055.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1734+1388_1734+139 others(8): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028495 | |||||
chr5:150028501
|
A | ATGTGTGT others(3): Show |
1 | a0004c0005t0001g0255 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1734+1387_1734+138 others(14): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028501 | |||||
chr5:150028501
|
A | ATGTGTGT others(5): Show |
2 | a0004c0005t0001g0250a0004c0005t0001g0251 | 2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1734+1387_1734+138 others(16): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028501 | |||||
chr5:150028501
|
A | G | 8 | a0001c0001t0001g0158a0001c0001t0001g0198a0001c0001t0001g0199others(5): Show | 8 | HG01256.hp1 HG02683.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.1734+1384A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028501 | ||||||
chr5:150028501
|
ATGTATG | A | 30 | a0001c0003t0001g0322a0001c0003t0005g0153a0001c0003t0006g0296others(27): Show | 35 | HG00099.hp1 HG00597.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.1734+1388_1734+139 others(10): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028501 | |||||
chr5:150028501
|
ATGTATGT others(1): Show |
A | 40 | a0001c0003t0001g0005a0001c0003t0001g0309a0001c0003t0001g0313others(37): Show | 50 | HG00544.hp1 HG00673.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.1734+1388_1734+139 others(12): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028501 | |||||
chr5:150028501
|
ATGTATGT others(3): Show |
A | 3 | a0001c0003t0001g0308a0001c0003t0005g0142a0001c0003t0008g0295 | 3 | HG02145.hp2 HG02280.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1734+1388_1734+139 others(14): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028501 | |||||
chr5:150028503
|
GTA | G | 5 | a0001c0001t0001g0238a0001c0003t0005g0034a0001c0003t0005g0285others(2): Show | 6 | HG00735.hp2 HG02258.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1734+1388_1734+138 others(6): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028503 | |||||
chr5:150028505
|
A | ATG | 6 | a0002c0002t0001g0016a0002c0002t0002g0039a0002c0002t0002g0055others(3): Show | 7 | HG02071.hp1 HG02698.hp1 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.1734+1424_1734+142 others(6): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028505 | |||||
chr5:150028505
|
A | ATGTGTG | 4 | a0001c0001t0011g0012a0001c0001t0011g0037a0001c0001t0011g0038others(1): Show | 4 | HG02630.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1734+1420_1734+142 others(10): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028505 | |||||
chr5:150028505
|
A | G | 150 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(147): Show | 160 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.1734+1388A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028505 | ||||||
chr5:150028505
|
ATG | A | 3 | a0002c0002t0002g0060a0002c0002t0002g0079a0002c0002t0023g0101 | 3 | HG03239.hp2 HG03669.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1734+1424_1734+142 others(6): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028505 | |||||
chr5:150028505
|
ATGTGTGT others(5): Show |
A | 2 | a0008c0011t0001g0033a0008c0011t0005g0033 | 2 | HG02896.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1734+1414_1734+142 others(16): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028505 | |||||
chr5:150028527
|
G | A | 1 | a0001c0003t0019g0288 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1734+1410G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028527 | ||||||
chr5:150028529
|
G | A | 1 | a0001c0003t0019g0288 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1734+1412G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028529 | ||||||
chr5:150028531
|
G | A | 3 | a0001c0003t0005g0282a0001c0003t0005g0283a0001c0003t0019g0288 | 3 | HG01891.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1734+1414G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028531 | ||||||
chr5:150028533
|
G | A | 8 | a0001c0003t0005g0034a0001c0003t0005g0282a0001c0003t0005g0283others(5): Show | 9 | HG00735.hp2 HG01891.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.1734+1416G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028533 | ||||||
chr5:150028535
|
G | A | 11 | a0001c0003t0005g0034a0001c0003t0005g0152a0001c0003t0005g0153others(8): Show | 12 | HG00735.hp2 HG01891.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.1734+1418G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028535 | ||||||
chr5:150028537
|
G | A | 12 | a0001c0001t0002g0209a0001c0003t0005g0034a0001c0003t0005g0152others(9): Show | 13 | HG00735.hp2 HG01891.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.1734+1420G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028537 | ||||||
chr5:150028539
|
G | A | 22 | a0001c0001t0001g0106a0001c0001t0001g0188a0001c0001t0002g0209others(19): Show | 24 | HG00735.hp2 HG01243.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.1734+1422G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028539 | ||||||
chr5:150028541
|
G | A | 50 | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0106others(47): Show | 59 | HG00597.hp2 HG00673.hp2 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.1734+1424G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028541 | ||||||
chr5:150028541
|
G | GTGTA | 3 | a0001c0001t0001g0162a0001c0001t0001g0243a0001c0001t0003g0212 | 3 | HG02683.hp1 NA18948.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1734+1425_1734+142 others(8): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028541 | |||||
chr5:150028541
|
G | GTGTGTA | 6 | a0001c0001t0001g0027a0001c0001t0001g0170a0001c0001t0001g0171others(3): Show | 6 | HG02896.hp2 HG02897.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.1734+1425_1734+142 others(10): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028541 | |||||
chr5:150028541
|
G | GTGTGTGT others(1): Show |
5 | a0001c0001t0001g0036a0001c0001t0001g0172a0004c0005t0001g0252others(2): Show | 5 | HG02080.hp1 HG06807.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.1734+1425_1734+142 others(12): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028541 | |||||
chr5:150028541
|
G | GTGTGTGT others(3): Show |
10 | a0004c0005t0001g0032a0004c0005t0001g0258a0004c0005t0001g0260others(7): Show | 11 | HG00639.hp1 HG01361.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.1734+1425_1734+142 others(14): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028541 | |||||
chr5:150028541
|
G | GTGTGTGT others(3): Show |
5 | a0001c0001t0003g0206a0004c0005t0001g0249a0004c0005t0001g0267others(2): Show | 5 | HG02258.hp1 HG02698.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1734+1425_1734+142 others(14): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028541 | |||||
chr5:150028541
|
G | GTGTGTGT others(5): Show |
5 | a0004c0005t0001g0266a0004c0005t0001g0269a0004c0005t0002g0277others(2): Show | 5 | HG01106.hp1 HG01255.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.1734+1425_1734+142 others(16): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028541 | |||||
chr5:150028543
|
A | G | 52 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0031others(49): Show | 59 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.1734+1426A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028543 | ||||||
chr5:150028545
|
A | G | 2 | a0001c0001t0001g0043a0001c0001t0006g0298 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1734+1428A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028545 | ||||||
chr5:150028555
|
ATATATTT others(3): Show |
A | 4 | a0001c0003t0006g0296a0001c0003t0006g0307a0001c0003t0008g0291others(1): Show | 4 | HG01884.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1734+1440_1734+144 others(14): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028555 | |||||
chr5:150028557
|
ATATTTTT others(1): Show |
A | 29 | a0001c0003t0001g0005a0001c0003t0001g0309a0001c0003t0001g0313others(26): Show | 31 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.1734+1442_1734+144 others(12): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028557 | |||||
chr5:150028559
|
A | AT | 8 | a0001c0001t0011g0012a0001c0001t0011g0037a0001c0001t0011g0038others(5): Show | 8 | HG02293.hp2 HG02630.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1734+1461dupT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028559 | |||||
chr5:150028559
|
A | ATAT | 7 | a0001c0001t0001g0043a0001c0001t0003g0193a0001c0001t0006g0298others(4): Show | 7 | HG01167.hp1 HG03453.hp2 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.1734+1443_1734+144 others(7): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028559 | |||||
chr5:150028559
|
A | T | 11 | a0001c0003t0005g0025a0001c0003t0005g0140a0001c0003t0005g0142others(8): Show | 14 | HG01243.hp2 HG02280.hp1 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.1734+1442A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028559 | ||||||
chr5:150028559
|
AT | A | 41 | a0001c0001t0001g0188a0001c0001t0003g0154a0001c0001t0003g0290others(38): Show | 53 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.1734+1461delT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028559 | |||||
chr5:150028559
|
ATTT | A | 9 | a0003c0004t0004g0022a0003c0004t0004g0127a0003c0004t0007g0024others(6): Show | 11 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.1734+1459_1734+146 others(7): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028559 | |||||
chr5:150028560
|
T | TA | 46 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0036others(43): Show | 51 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.1734+1443_1734+144 others(5): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028560 | ||||||
chr5:150028560
|
T | TATA | 52 | a0001c0001t0001g0003a0001c0001t0001g0157a0001c0001t0001g0158others(49): Show | 57 | HG00140.hp1 HG00544.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.1734+1443_1734+144 others(7): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028560 | ||||||
chr5:150028560
|
T | TATATA | 33 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0031others(30): Show | 37 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1734+1443_1734+144 others(9): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028560 | ||||||
chr5:150028560
|
T | TATATATA | 3 | a0004c0005t0001g0256a0004c0005t0001g0257a0004c0005t0001g0259 | 3 | HG02074.hp2 HG03710.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1734+1443_1734+144 others(11): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028560 | ||||||
chr5:150028561
|
T | A | 22 | a0001c0001t0001g0018a0001c0001t0001g0106a0001c0001t0001g0162others(19): Show | 24 | HG01106.hp1 HG01243.hp2 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.1734+1444T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028561 | ||||||
chr5:150028562
|
T | A | 63 | a0001c0001t0001g0231a0001c0001t0003g0226a0001c0001t0011g0149others(60): Show | 79 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.1734+1445T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028562 | ||||||
chr5:150028563
|
T | A | 8 | a0001c0001t0001g0018a0001c0001t0001g0106a0001c0003t0005g0152others(5): Show | 9 | HG01106.hp1 HG02055.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1734+1446T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028563 | ||||||
chr5:150028564
|
T | A | 16 | a0002c0002t0002g0090a0003c0004t0004g0124a0004c0005t0001g0032others(13): Show | 17 | HG02074.hp2 HG02132.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1734+1447T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028564 | ||||||
chr5:150028565
|
T | A | 2 | a0001c0003t0001g0308a0004c0005t0001g0274 | 2 | HG03098.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1734+1448T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028565 | ||||||
chr5:150028566
|
T | A | 1 | a0004c0005t0001g0266 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1734+1449T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028566 | ||||||
chr5:150028584
|
A | G | 1 | a0015c0015t0005g0111 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1734+1467A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028584 | ||||||
chr5:150028615
|
G | A | 2 | a0008c0011t0001g0033a0008c0011t0005g0033 | 2 | HG02896.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1734+1498G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028615 | ||||||
chr5:150028694
|
G | A | 1 | a0001c0021t0006g0294 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1734+1577G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028694 | ||||||
chr5:150028714
|
G | C | 2 | a0002c0002t0002g0013a0002c0002t0002g0054 | 3 | HG01257.hp2 HG01258.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.1734+1597G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028714 | ||||||
chr5:150029009
|
C | T | 3 | a0001c0001t0001g0031a0001c0001t0001g0243a0001c0001t0003g0159 | 4 | NA18948.hp2 NA18950.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.1735-1732C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150029009 | ||||||
chr5:150029018
|
A | G | 109 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(106): Show | 118 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.1735-1723A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150029018 | ||||||
chr5:150029133
|
T | A | 1 | a0002c0002t0002g0060 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1735-1608T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150029133 | ||||||
chr5:150029330
|
G | GT | 118 | a0001c0001t0001g0018a0001c0001t0001g0043a0001c0001t0001g0106others(115): Show | 139 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.1735-1395dupT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150029330 | |||||
chr5:150029366
|
G | A | 52 | a0001c0003t0005g0025a0001c0003t0005g0034a0001c0003t0005g0140others(49): Show | 67 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.1735-1375G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150029366 | ||||||
chr5:150029731
|
C | T | 243 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(240): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1735-1010C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150029731 | ||||||
chr5:150029901
|
G | A | 6 | a0001c0001t0001g0018a0001c0001t0001g0106a0005c0006t0005g0008others(3): Show | 11 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.1735-840G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150029901 | ||||||
chr5:150029974
|
T | C | 1 | a0001c0001t0003g0176 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1735-767T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150029974 | ||||||
chr5:150029994
|
T | C | 1 | a0001c0003t0001g0313 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1735-747T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150029994 | ||||||
chr5:150030134
|
TTTTC | T | 86 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(83): Show | 103 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.1735-599_1735-596d others(6): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150030134 | |||||
chr5:150030210
|
T | A | 89 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(86): Show | 106 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.1735-531T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150030210 | ||||||
chr5:150030579
|
T | C | 1 | a0001c0001t0003g0186 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1735-162T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150030579 | ||||||
chr5:150030590
|
T | G | 89 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(86): Show | 106 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.1735-151T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150030590 | ||||||
chr5:150030669
|
C | T | 3 | a0008c0011t0001g0033a0008c0011t0005g0033a0012c0020t0001g0292 | 3 | HG02896.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1735-72C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150030669 | ||||||
chr5:150030721
|
T | G | 1 | a0001c0001t0001g0194 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1735-20T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150030721 | ||||||
chr5:150030925
|
G | A | 2 | a0001c0001t0002g0161a0001c0001t0002g0163 | 2 | HG01071.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1833+86G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | chr5 | 150030925 | ||||||
chr5:150030956
|
A | C | 56 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(53): Show | 73 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.1833+117A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | chr5 | 150030956 | ||||||
chr5:150030977
|
AAGAT | A | 3 | a0008c0011t0001g0033a0008c0011t0005g0033a0012c0020t0001g0292 | 3 | HG02896.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1833+139_1833+142d others(6): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | chr5 | 150030977 | ||||||
chr5:150031180
|
C | A | 5 | a0001c0001t0003g0192a0001c0001t0003g0204a0001c0001t0003g0214others(2): Show | 5 | HG00639.hp2 HG01109.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.1833+341C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | chr5 | 150031180 | ||||||
chr5:150031301
|
C | G | 1 | a0003c0010t0004g0130 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1833+462C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | chr5 | 150031301 | ||||||
chr5:150031339
|
C | A | 9 | a0001c0003t0005g0034a0001c0003t0005g0282a0001c0003t0005g0283others(6): Show | 10 | HG00735.hp2 HG01891.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.1833+500C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | chr5 | 150031339 | ||||||
chr5:150031349
|
G | C | 5 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(2): Show | 7 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1833+510G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | chr5 | 150031349 | ||||||
chr5:150031417
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1833+578G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | chr5 | 150031417 | ||||||
chr5:150031470
|
A | G | 10 | a0001c0001t0001g0043a0001c0001t0001g0150a0001c0001t0001g0151others(7): Show | 10 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1833+631A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | chr5 | 150031470 | ||||||
chr5:150031609
|
G | C | 2 | a0008c0011t0001g0033a0008c0011t0005g0033 | 2 | HG02896.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1833+770G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | chr5 | 150031609 | ||||||
chr5:150032038
|
T | C | 1 | a0001c0001t0001g0158 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1834-416T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | chr5 | 150032038 | ||||||
chr5:150032088
|
TTTGTCTT others(16): Show |
T | 2 | a0001c0003t0005g0318a0001c0003t0005g0319 | 2 | HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1834-364_1834-342d others(25): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr5 | 150032088 | |||||
chr5:150032260
|
C | T | 1 | a0001c0001t0003g0225 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1834-194C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | chr5 | 150032260 | ||||||
chr5:150032387
|
T | C | 1 | a0001c0001t0002g0209 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1834-67T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | chr5 | 150032387 | ||||||
chr5:150032425
|
A | G | 1 | a0001c0001t0003g0241 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1834-29A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | chr5 | 150032425 | ||||||
chr5:150032668
|
G | A | 1 | a0004c0005t0001g0259 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1983+65G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150032668 | ||||||
chr5:150032747
|
A | T | 1 | a0012c0020t0001g0292 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1983+144A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150032747 | ||||||
chr5:150032808
|
A | G | 1 | a0002c0002t0002g0068 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1983+205A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150032808 | ||||||
chr5:150032884
|
A | G | 37 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(34): Show | 39 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(36): Show |
intron_variant | MODIFIER | c.1983+281A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150032884 | ||||||
chr5:150032982
|
G | A | 246 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0018others(243): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.1983+379G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150032982 | ||||||
chr5:150033215
|
A | G | 54 | a0001c0003t0005g0025a0001c0003t0005g0034a0001c0003t0005g0140others(51): Show | 69 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.1983+612A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150033215 | ||||||
chr5:150033292
|
G | A | 18 | a0001c0003t0005g0025a0001c0003t0005g0034a0001c0003t0005g0140others(15): Show | 20 | HG00735.hp2 HG01243.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1983+689G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150033292 | ||||||
chr5:150033368
|
G | A | 4 | a0001c0001t0011g0012a0001c0001t0011g0037a0001c0001t0011g0038others(1): Show | 4 | HG02630.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1983+765G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150033368 | ||||||
chr5:150033553
|
C | T | 1 | a0002c0014t0002g0067 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1983+950C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150033553 | ||||||
chr5:150033598
|
G | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0106 | 3 | HG02451.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1983+995G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150033598 | ||||||
chr5:150033623
|
A | G | 248 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0018others(245): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1983+1020A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150033623 | ||||||
chr5:150033878
|
G | T | 54 | a0001c0003t0005g0025a0001c0003t0005g0034a0001c0003t0005g0140others(51): Show | 69 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.1983+1275G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150033878 | ||||||
chr5:150034047
|
T | G | 143 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(140): Show | 153 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1983+1444T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150034047 | ||||||
chr5:150034096
|
T | C | 91 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(88): Show | 108 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.1983+1493T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150034096 | ||||||
chr5:150034435
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1983+1832G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150034435 | ||||||
chr5:150034446
|
C | T | 1 | a0001c0003t0019g0288 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1983+1843C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150034446 | ||||||
chr5:150034453
|
C | T | 1 | a0002c0002t0003g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1983+1850C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150034453 | ||||||
chr5:150034454
|
G | A | 54 | a0001c0003t0005g0025a0001c0003t0005g0034a0001c0003t0005g0140others(51): Show | 69 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.1983+1851G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150034454 | ||||||
chr5:150034455
|
C | T | 9 | a0001c0001t0001g0043a0001c0001t0001g0150a0001c0001t0001g0151others(6): Show | 9 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1983+1852C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150034455 | ||||||
chr5:150034481
|
T | C | 1 | a0001c0003t0005g0318 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1983+1878T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150034481 | ||||||
chr5:150034512
|
C | T | 20 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(17): Show | 22 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1983+1909C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150034512 | ||||||
chr5:150034678
|
A | G | 2 | a0001c0003t0006g0302a0001c0003t0006g0303 | 2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1984-1958A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150034678 | ||||||
chr5:150034732
|
T | C | 4 | a0002c0002t0001g0110a0002c0002t0002g0019a0002c0002t0002g0108others(1): Show | 5 | NA18941.hp1 NA18989.hp1 NA19078.hp1 others(2): Show |
intron_variant | MODIFIER | c.1984-1904T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150034732 | ||||||
chr5:150034812
|
A | T | 1 | a0001c0003t0006g0293 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1984-1824A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150034812 | ||||||
chr5:150034859
|
G | T | 3 | a0001c0003t0005g0142a0001c0003t0005g0143a0001c0019t0005g0144 | 3 | HG02280.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1984-1777G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150034859 | ||||||
chr5:150035009
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0006g0298 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1984-1627G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035009 | ||||||
chr5:150035048
|
C | T | 2 | a0001c0003t0003g0311a0001c0003t0003g0312 | 2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1984-1588C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035048 | ||||||
chr5:150035076
|
G | T | 2 | a0001c0003t0006g0304a0001c0021t0006g0294 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1984-1560G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035076 | ||||||
chr5:150035089
|
A | G | 36 | a0003c0004t0004g0001a0003c0004t0004g0010a0003c0004t0004g0020others(33): Show | 49 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1984-1547A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035089 | ||||||
chr5:150035107
|
C | T | 1 | a0001c0003t0019g0288 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1984-1529C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035107 | ||||||
chr5:150035176
|
G | A | 6 | a0001c0003t0005g0025a0001c0003t0005g0140a0001c0003t0005g0142others(3): Show | 7 | HG01243.hp2 HG02280.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1984-1460G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035176 | ||||||
chr5:150035336
|
A | G | 244 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(241): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1984-1300A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035336 | ||||||
chr5:150035382
|
T | C | 2 | a0001c0001t0005g0227a0010c0027t0001g0230 | 2 | HG02074.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1984-1254T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035382 | ||||||
chr5:150035446
|
G | A | 12 | a0001c0003t0005g0034a0001c0003t0005g0152a0001c0003t0005g0153others(9): Show | 13 | HG00735.hp2 HG01891.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.1984-1190G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035446 | ||||||
chr5:150035532
|
A | G | 54 | a0001c0003t0005g0025a0001c0003t0005g0034a0001c0003t0005g0140others(51): Show | 69 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.1984-1104A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035532 | ||||||
chr5:150035646
|
T | A | 1 | a0015c0015t0005g0111 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1984-990T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035646 | ||||||
chr5:150035656
|
G | A | 213 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(210): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1984-980G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035656 | ||||||
chr5:150035683
|
G | T | 4 | a0001c0001t0011g0012a0001c0001t0011g0037a0001c0001t0011g0038others(1): Show | 4 | HG02630.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1984-953G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035683 | ||||||
chr5:150035838
|
A | G | 144 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(141): Show | 154 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.1984-798A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035838 | ||||||
chr5:150035995
|
A | G | 91 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(88): Show | 108 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.1984-641A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035995 | ||||||
chr5:150036042
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1984-594A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150036042 | ||||||
chr5:150036967
|
A | T | 1 | a0002c0002t0002g0053 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2285+30A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 12/19 | chr5 | 150036967 | ||||||
chr5:150037575
|
G | T | 55 | a0001c0003t0005g0025a0001c0003t0005g0034a0001c0003t0005g0140others(52): Show | 70 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.2413+48G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150037575 | ||||||
chr5:150037980
|
C | T | 2 | a0002c0002t0002g0045a0002c0002t0002g0046 | 2 | HG02132.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2413+453C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150037980 | ||||||
chr5:150037989
|
C | T | 89 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(86): Show | 106 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.2413+462C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150037989 | ||||||
chr5:150038190
|
C | A | 6 | a0001c0001t0001g0018a0001c0001t0001g0106a0005c0006t0005g0008others(3): Show | 11 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.2413+663C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150038190 | ||||||
chr5:150038268
|
T | G | 4 | a0001c0001t0011g0012a0001c0001t0011g0037a0001c0001t0011g0038others(1): Show | 4 | HG02630.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2413+741T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150038268 | ||||||
chr5:150038563
|
A | G | 92 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(89): Show | 109 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.2413+1036A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150038563 | ||||||
chr5:150038761
|
G | A | 1 | a0001c0001t0003g0177 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2413+1234G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150038761 | ||||||
chr5:150038849
|
A | G | 4 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(1): Show | 6 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2413+1322A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150038849 | ||||||
chr5:150039135
|
G | T | 1 | a0003c0004t0004g0325 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2413+1608G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150039135 | ||||||
chr5:150039453
|
G | T | 9 | a0001c0001t0001g0043a0001c0001t0001g0150a0001c0001t0001g0151others(6): Show | 9 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2414-1295G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150039453 | ||||||
chr5:150039487
|
G | A | 2 | a0001c0003t0006g0304a0001c0021t0006g0294 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2414-1261G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150039487 | ||||||
chr5:150039625
|
T | C | 89 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(86): Show | 106 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.2414-1123T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150039625 | ||||||
chr5:150039713
|
A | C | 2 | a0001c0003t0005g0286a0001c0003t0005g0289 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2414-1035A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150039713 | ||||||
chr5:150039734
|
C | T | 248 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0018others(245): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.2414-1014C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150039734 | ||||||
chr5:150039759
|
C | CTT | 92 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(89): Show | 109 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.2414-986_2414-985d others(4): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 150039759 | |||||
chr5:150039784
|
A | G | 4 | a0003c0004t0004g0001a0003c0004t0004g0116a0003c0004t0004g0122others(1): Show | 10 | HG01433.hp2 HG01496.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.2414-964A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150039784 | ||||||
chr5:150039846
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0106 | 3 | HG02451.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2414-902C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150039846 | ||||||
chr5:150039863
|
C | T | 20 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(17): Show | 22 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.2414-885C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150039863 | ||||||
chr5:150040028
|
C | T | 14 | a0001c0003t0001g0313a0001c0003t0001g0317a0001c0003t0001g0320others(11): Show | 14 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2414-720C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150040028 | ||||||
chr5:150040172
|
G | A | 3 | a0008c0011t0001g0033a0008c0011t0005g0033a0012c0020t0001g0292 | 3 | HG02896.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2414-576G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150040172 | ||||||
chr5:150040222
|
A | G | 2 | a0007c0009t0004g0129a0007c0009t0004g0132 | 2 | HG02280.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2414-526A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150040222 | ||||||
chr5:150040229
|
G | A | 56 | a0001c0003t0005g0025a0001c0003t0005g0034a0001c0003t0005g0140others(53): Show | 71 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.2414-519G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150040229 | ||||||
chr5:150040257
|
A | T | 3 | a0008c0011t0001g0033a0008c0011t0005g0033a0012c0020t0001g0292 | 3 | HG02896.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2414-491A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150040257 | ||||||
chr5:150040428
|
C | T | 89 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(86): Show | 106 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.2414-320C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150040428 | ||||||
chr5:150040584
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2414-164C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150040584 | ||||||
chr5:150040595
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2414-153C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150040595 | ||||||
chr5:150040600
|
A | G | 18 | a0001c0003t0005g0025a0001c0003t0005g0034a0001c0003t0005g0140others(15): Show | 20 | HG00735.hp2 HG01243.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.2414-148A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150040600 | ||||||
chr5:150040617
|
A | C | 12 | a0001c0003t0005g0034a0001c0003t0005g0152a0001c0003t0005g0153others(9): Show | 13 | HG00735.hp2 HG01891.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.2414-131A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150040617 | ||||||
chr5:150040742
|
C | T | 4 | a0003c0004t0004g0020a0003c0004t0004g0115a0003c0004t0004g0119others(1): Show | 5 | NA18971.hp1 NA18997.hp1 NA19012.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.2414-6C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150040742 | ||||||
chr5:150040928
|
G | A | 1 | a0001c0003t0005g0287 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2545+49G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 14/19 | chr5 | 150040928 | ||||||
chr5:150040990
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2545+111A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 14/19 | chr5 | 150040990 | ||||||
chr5:150040996
|
A | C | 3 | a0002c0002t0002g0085a0002c0002t0002g0096a0002c0002t0002g0097 | 3 | NA18950.hp2 NA18982.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2545+117A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 14/19 | chr5 | 150040996 | ||||||
chr5:150041126
|
C | A | 1 | a0003c0004t0004g0117 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2545+247C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 14/19 | chr5 | 150041126 | ||||||
chr5:150041135
|
G | T | 69 | a0001c0003t0001g0313a0001c0003t0001g0317a0001c0003t0001g0320others(66): Show | 84 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.2545+256G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 14/19 | chr5 | 150041135 | ||||||
chr5:150041153
|
C | T | 12 | a0001c0003t0005g0034a0001c0003t0005g0152a0001c0003t0005g0153others(9): Show | 13 | HG00735.hp2 HG01891.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.2545+274C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 14/19 | chr5 | 150041153 | ||||||
chr5:150041154
|
C | G | 1 | a0003c0004t0007g0113 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2545+275C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 14/19 | chr5 | 150041154 | ||||||
chr5:150041187
|
C | T | 1 | a0002c0002t0002g0147 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2545+308C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 14/19 | chr5 | 150041187 | ||||||
chr5:150041434
|
G | A | 3 | a0008c0011t0001g0033a0008c0011t0005g0033a0012c0020t0001g0292 | 3 | HG02896.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2546-351G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 14/19 | chr5 | 150041434 | ||||||
chr5:150041548
|
G | A | 2 | a0001c0003t0001g0317a0001c0003t0001g0320 | 2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2546-237G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 14/19 | chr5 | 150041548 | ||||||
chr5:150041603
|
T | C | 1 | a0002c0002t0002g0076 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2546-182T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 14/19 | chr5 | 150041603 | ||||||
chr5:150041990
|
G | T | 1 | a0001c0001t0002g0218 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2730+21G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150041990 | ||||||
chr5:150042002
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0232 | 2 | NA18946.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.2730+33C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150042002 | ||||||
chr5:150042003
|
G | A | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200 | 3 | NA18954.hp1 NA18983.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.2730+34G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150042003 | ||||||
chr5:150042024
|
C | T | 2 | a0008c0011t0001g0033a0008c0011t0005g0033 | 2 | HG02896.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2730+55C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150042024 | ||||||
chr5:150042224
|
T | C | 1 | a0001c0003t0008g0295 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2730+255T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150042224 | ||||||
chr5:150042271
|
T | C | 4 | a0002c0002t0002g0007a0002c0002t0002g0015a0002c0002t0002g0073others(1): Show | 7 | HG01106.hp2 HG01952.hp1 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.2730+302T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150042271 | ||||||
chr5:150042284
|
T | G | 143 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(140): Show | 153 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.2730+315T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150042284 | ||||||
chr5:150042852
|
A | C | 1 | a0001c0001t0003g0225 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2730+883A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150042852 | ||||||
chr5:150042964
|
A | G | 32 | a0001c0003t0001g0313a0001c0003t0001g0317a0001c0003t0001g0320others(29): Show | 34 | HG00735.hp2 HG01243.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.2730+995A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150042964 | ||||||
chr5:150043040
|
G | C | 142 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(139): Show | 152 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.2730+1071G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150043040 | ||||||
chr5:150043095
|
C | G | 5 | a0001c0003t0005g0310a0001c0003t0005g0315a0001c0003t0005g0318others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2730+1126C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150043095 | ||||||
chr5:150043099
|
A | G | 1 | a0012c0020t0001g0292 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2730+1130A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150043099 | ||||||
chr5:150043107
|
G | A | 1 | a0001c0001t0001g0201 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2730+1138G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150043107 | ||||||
chr5:150043173
|
G | A | 4 | a0002c0002t0002g0040a0002c0002t0002g0074a0002c0002t0002g0075others(1): Show | 4 | NA18612.hp2 NA18942.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.2730+1204G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150043173 | ||||||
chr5:150043306
|
ACACT | A | 31 | a0001c0003t0001g0313a0001c0003t0001g0317a0001c0003t0001g0320others(28): Show | 33 | HG00735.hp2 HG01243.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.2730+1341_2730+134 others(8): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr5 | 150043306 | |||||
chr5:150043423
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2730+1454G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150043423 | ||||||
chr5:150043636
|
C | T | 105 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(102): Show | 114 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.2730+1667C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150043636 | ||||||
chr5:150043817
|
A | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0106 | 3 | HG02451.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2731-1649A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150043817 | ||||||
chr5:150043876
|
C | T | 1 | a0001c0001t0003g0204 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2731-1590C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150043876 | ||||||
chr5:150043893
|
C | T | 3 | a0008c0011t0001g0033a0008c0011t0005g0033a0012c0020t0001g0292 | 3 | HG02896.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2731-1573C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150043893 | ||||||
chr5:150044101
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2731-1365C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150044101 | ||||||
chr5:150044276
|
G | A | 14 | a0001c0003t0001g0313a0001c0003t0001g0317a0001c0003t0001g0320others(11): Show | 14 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2731-1190G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150044276 | ||||||
chr5:150044447
|
GGT | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0106 | 3 | HG02451.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2731-1017_2731-101 others(6): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr5 | 150044447 | |||||
chr5:150044476
|
G | A | 1 | a0001c0003t0005g0285 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2731-990G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150044476 | ||||||
chr5:150044524
|
C | T | 2 | a0004c0005t0001g0263a0004c0005t0001g0269 | 2 | NA18979.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.2731-942C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150044524 | ||||||
chr5:150044659
|
C | T | 14 | a0001c0003t0001g0313a0001c0003t0001g0317a0001c0003t0001g0320others(11): Show | 14 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2731-807C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150044659 | ||||||
chr5:150044740
|
A | G | 1 | a0002c0002t0002g0014 | 2 | NA18971.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.2731-726A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150044740 | ||||||
chr5:150044819
|
T | G | 3 | a0008c0011t0001g0033a0008c0011t0005g0033a0012c0020t0001g0292 | 3 | HG02896.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2731-647T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150044819 | ||||||
chr5:150044866
|
A | G | 3 | a0008c0011t0001g0033a0008c0011t0005g0033a0012c0020t0001g0292 | 3 | HG02896.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2731-600A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150044866 | ||||||
chr5:150044945
|
C | T | 33 | a0001c0001t0001g0162a0004c0005t0001g0032a0004c0005t0001g0249others(30): Show | 34 | HG00639.hp1 HG01106.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.2731-521C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150044945 | ||||||
chr5:150045403
|
G | A | 246 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0018others(243): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.2731-63G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150045403 | ||||||
chr5:150045445
|
T | A | 3 | a0002c0002t0001g0016a0002c0002t0002g0080a0009c0028t0002g0086 | 4 | NA18973.hp1 NA19007.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.2731-21T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150045445 | ||||||
chr5:150045915
|
G | A | 1 | a0015c0015t0005g0111 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2950+230G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150045915 | ||||||
chr5:150045966
|
C | T | 1 | a0001c0021t0006g0294 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2950+281C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150045966 | ||||||
chr5:150046225
|
C | T | 72 | a0001c0003t0001g0313a0001c0003t0001g0317a0001c0003t0001g0320others(69): Show | 87 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.2950+540C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150046225 | ||||||
chr5:150046277
|
G | A | 1 | a0002c0002t0002g0100 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2950+592G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150046277 | ||||||
chr5:150046322
|
A | G | 9 | a0001c0001t0001g0043a0001c0001t0001g0150a0001c0001t0001g0151others(6): Show | 9 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2950+637A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150046322 | ||||||
chr5:150046340
|
C | T | 69 | a0001c0003t0001g0313a0001c0003t0001g0317a0001c0003t0001g0320others(66): Show | 84 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.2950+655C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150046340 | ||||||
chr5:150046483
|
T | C | 1 | a0007c0009t0004g0131 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2950+798T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150046483 | ||||||
chr5:150046629
|
G | A | 3 | a0001c0003t0006g0307a0001c0003t0008g0291a0001c0003t0030g0306 | 3 | HG02886.hp1 HG02895.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2950+944G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150046629 | ||||||
chr5:150046744
|
G | A | 37 | a0002c0014t0002g0067a0003c0004t0004g0001a0003c0004t0004g0010others(34): Show | 50 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2951-880G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150046744 | ||||||
chr5:150046767
|
G | A | 1 | a0015c0015t0005g0111 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2951-857G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150046767 | ||||||
chr5:150046799
|
G | A | 2 | a0008c0011t0001g0033a0008c0011t0005g0033 | 2 | HG02896.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2951-825G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150046799 | ||||||
chr5:150046807
|
G | A | 1 | a0001c0001t0003g0221 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2951-817G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150046807 | ||||||
chr5:150046891
|
C | CT | 20 | a0001c0001t0003g0205a0001c0003t0001g0005a0001c0003t0001g0308others(17): Show | 22 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.2951-721dupT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr5 | 150046891 | |||||
chr5:150046891
|
C | CTT | 14 | a0001c0003t0001g0313a0001c0003t0001g0317a0001c0003t0001g0320others(11): Show | 14 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2951-722_2951-721d others(4): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr5 | 150046891 | |||||
chr5:150046908
|
C | T | 1 | a0004c0005t0001g0267 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2951-716C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150046908 | ||||||
chr5:150046977
|
C | T | 1 | a0015c0015t0005g0111 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2951-647C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150046977 | ||||||
chr5:150047024
|
A | G | 1 | a0012c0020t0001g0292 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2951-600A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150047024 | ||||||
chr5:150047033
|
C | T | 8 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0006g0298others(5): Show | 8 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2951-591C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150047033 | ||||||
chr5:150047044
|
C | A | 1 | a0001c0001t0001g0188 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2951-580C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150047044 | ||||||
chr5:150047185
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2951-439C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150047185 | ||||||
chr5:150047387
|
T | G | 4 | a0001c0001t0011g0012a0001c0001t0011g0037a0001c0001t0011g0038others(1): Show | 4 | HG02630.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2951-237T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150047387 | ||||||
chr5:150047403
|
A | G | 321 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0018others(318): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.2951-221A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150047403 | ||||||
chr5:150047420
|
C | G | 1 | a0002c0002t0003g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2951-204C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150047420 | ||||||
chr5:150047447
|
G | C | 333 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0018others(330): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.2951-177G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150047447 | ||||||
chr5:150047505
|
A | G | 1 | a0003c0004t0007g0024 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2951-119A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150047505 | ||||||
chr5:150047824
|
T | G | 333 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0018others(330): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.3084+67T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 17/19 | chr5 | 150047824 | ||||||
chr5:150047972
|
G | A | 1 | a0002c0002t0003g0077 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.3084+215G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 17/19 | chr5 | 150047972 | ||||||
chr5:150047980
|
G | A | 91 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(88): Show | 108 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.3084+223G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 17/19 | chr5 | 150047980 | ||||||
chr5:150048179
|
A | C | 1 | a0003c0004t0004g0124 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3085-390A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 17/19 | chr5 | 150048179 | ||||||
chr5:150048187
|
A | G | 1 | a0002c0002t0002g0146 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.3085-382A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 17/19 | chr5 | 150048187 | ||||||
chr5:150048400
|
T | TTGCTTAC others(9): Show |
88 | a0001c0003t0001g0005a0001c0003t0001g0308a0001c0003t0001g0309others(85): Show | 105 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.3085-168_3085-153d others(18): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr5 | 150048400 | |||||
chr5:150048533
|
C | T | 14 | a0001c0003t0001g0313a0001c0003t0001g0317a0001c0003t0001g0320others(11): Show | 14 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.3085-36C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 17/19 | chr5 | 150048533 | ||||||
chr5:150048541
|
T | C | 1 | a0010c0027t0001g0230 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.3085-28T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 17/19 | chr5 | 150048541 | ||||||
chr5:150048768
|
G | A | 1 | a0004c0005t0001g0272 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3201+83G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150048768 | ||||||
chr5:150048768
|
G | T | 3 | a0007c0009t0004g0129a0007c0009t0004g0131a0007c0009t0004g0132 | 3 | HG02280.hp2 HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3201+83G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150048768 | ||||||
chr5:150048799
|
C | T | 1 | a0001c0001t0026g0208 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3201+114C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150048799 | ||||||
chr5:150048817
|
G | A | 1 | a0001c0003t0019g0288 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3201+132G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150048817 | ||||||
chr5:150048832
|
C | G | 250 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0018others(247): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.3201+147C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150048832 | ||||||
chr5:150048835
|
G | A | 14 | a0001c0003t0001g0313a0001c0003t0001g0317a0001c0003t0001g0320others(11): Show | 14 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.3201+150G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150048835 | ||||||
chr5:150048861
|
G | C | 217 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(214): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.3201+176G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150048861 | ||||||
chr5:150048968
|
G | A | 11 | a0001c0003t0005g0034a0001c0003t0005g0152a0001c0003t0005g0153others(8): Show | 12 | HG00735.hp2 HG01891.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.3201+283G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150048968 | ||||||
chr5:150048970
|
A | G | 1 | a0015c0015t0005g0111 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3201+285A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150048970 | ||||||
chr5:150049002
|
T | C | 1 | a0002c0002t0002g0074 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3201+317T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150049002 | ||||||
chr5:150049299
|
G | A | 1 | a0001c0003t0005g0025 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3201+614G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150049299 | ||||||
chr5:150049327
|
A | G | 252 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0018others(249): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.3201+642A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150049327 | ||||||
chr5:150049410
|
A | AC | 146 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(143): Show | 156 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.3201+734dupC | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 150049410 | |||||
chr5:150049575
|
C | T | 4 | a0005c0006t0005g0008a0005c0006t0009g0009a0005c0006t0009g0105others(1): Show | 8 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.3202-677C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150049575 | ||||||
chr5:150049646
|
C | T | 160 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0018others(157): Show | 175 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.3202-606C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150049646 | ||||||
chr5:150049693
|
T | C | 14 | a0001c0003t0001g0313a0001c0003t0001g0317a0001c0003t0001g0320others(11): Show | 14 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.3202-559T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150049693 | ||||||
chr5:150049726
|
TGTGGAAT others(21): Show |
T | 1 | a0012c0020t0001g0292 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3202-520_3202-493d others(30): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 150049726 | |||||
chr5:150049777
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A | G | 8 | a0001c0001t0001g0043a0001c0001t0006g0298a0001c0001t0011g0012others(5): Show | 8 | HG02630.hp2 HG02886.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.3202-475A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150049777 | ||||||
chr5:150049976
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G | C | 1 | a0015c0015t0005g0111 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3202-276G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150049976 | ||||||
chr5:150050170
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G | A | 18 | a0001c0001t0001g0043a0001c0003t0001g0005a0001c0003t0001g0308others(15): Show | 20 | HG02109.hp2 HG02145.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.3202-82G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150050170 | ||||||
chr5:150050527
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G | A | 6 | a0002c0002t0001g0081a0002c0002t0005g0004a0002c0002t0005g0047others(3): Show | 8 | NA18939.hp2 NA18954.hp2 NA18965.hp2 others(5): Show |
intron_variant | MODIFIER | c.3411+66G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150050527 | ||||||
chr5:150050762
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T | G | 33 | a0001c0001t0001g0043a0001c0003t0001g0005a0001c0003t0001g0308others(30): Show | 35 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(32): Show |
intron_variant | MODIFIER | c.3411+301T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150050762 | ||||||
chr5:150050773
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G | T | 3 | a0008c0011t0001g0033a0008c0011t0005g0033a0012c0020t0001g0292 | 3 | HG02896.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3411+312G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150050773 | ||||||
chr5:150050928
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A | G | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200 | 3 | NA18954.hp1 NA18983.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.3411+467A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150050928 | ||||||
chr5:150051071
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C | T | 36 | a0001c0003t0005g0025a0001c0003t0005g0140a0001c0003t0005g0142others(33): Show | 49 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.3411+610C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150051071 | ||||||
chr5:150051094
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A | T | 111 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(108): Show | 120 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.3412-631A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150051094 | ||||||
chr5:150051352
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T | C | 116 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(113): Show | 125 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.3412-373T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150051352 | ||||||
chr5:150051445
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C | A | 31 | a0001c0003t0006g0299a0003c0004t0004g0001a0003c0004t0004g0010others(28): Show | 43 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.3412-280C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150051445 | ||||||
chr5:150051462
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C | T | 135 | a0001c0001t0001g0018a0001c0001t0001g0043a0001c0001t0001g0106others(132): Show | 159 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(156): Show |
intron_variant | MODIFIER | c.3412-263C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150051462 | ||||||
chr5:150051487
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G | A | 1 | a0001c0001t0003g0205 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3412-238G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150051487 | ||||||
chr5:150051606
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A | G | 7 | a0001c0003t0005g0025a0001c0003t0005g0140a0001c0003t0005g0142others(4): Show | 8 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.3412-119A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150051606 | ||||||
chr5:150051615
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T | A | 51 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0162others(48): Show | 53 | HG00735.hp2 HG01891.hp1 HG01981.hp2 others(50): Show |
intron_variant | MODIFIER | c.3412-110T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150051615 | ||||||
chr5:150051630
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A | G | 7 | a0001c0003t0005g0025a0001c0003t0005g0140a0001c0003t0005g0142others(4): Show | 8 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.3412-95A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150051630 | ||||||
chr5:150051660
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G | A | 244 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0018others(241): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.3412-65G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150051660 | ||||||
chr5:150051696
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A | G | 245 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0018others(242): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.3412-29A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150051696 |